Three-dimensional model of a Fc region of an IgE antibody and uses thereof

ABSTRACT

The present invention includes three-dimensional models of antibodies, such as Fc-Cε3/Cε4 regions of IgE antibodies, as well as methods to produce such models. The present invention also includes muteins having increased stability and/or antibody receptor binding activity, as well as methods to produce such muteins, preferably using information derived from three-dimensional models of the present invention. Also included are nucleic acid sequences encoding muteins of the present invention and use of those sequences to produce such muteins. Also included is the use of the model to identify compounds that inhibit the binding of an antibody receptor protein to an antibody. The present invention also includes uses of such muteins and inhibitory compounds, for example, in methods to diagnose and protect animals from allergy and other abnormal immune responses.

CROSS-REFERENCE TO RELATED APPLICATIONS

[0001] This Application claims priority to provisional application U.S. Ser. No. 60/189,403, filed Mar. 15, 2000, entitled THREE-DIMENSIONAL MODEL OF A Fc REGION OF AN IgE ANTIBODY AND USES THEREOF; and provisional application U.S. Ser. No. 60/234,877, filed Sep. 22, 2000, entitled “STRUCTURE OF THE HUMAN IgE-Fc Cε3-Cε4 REVEALS CONFORMATIONAL FLEXIBILITY IN THE ANTIBODY EFFECTOR DOMAINS.”

[0002] This invention was made at least in part with government support under NIH Grant No. RO1 AI38972, awarded by the National Institutes of Health to Northwestern University. The government has certain rights to this invention.

FIELD OF THE INVENTION

[0003] The present invention relates to a crystal and a three-dimensional (3-D) model of a constant region of an IgE antibody that includes the Cε3 and Cε4 domains (Fc-Cε3/Cε4, or Fc-Ce3/Ce4, region). The present invention also relates to the use of that model to produce muteins and inhibitors useful in the diagnosis and treatment of allergy and the regulation of other immune responses in an animal.

BACKGROUND OF THE INVENTION

[0004] Antibody Fc-receptors (FcRs) play an important role in the immune response by coupling the specificity of secreted antibodies to a variety of cells of the immune system. A number of cell types, including macrophages, mast cells, eosinophils, and basophils, express membrane-bound FcRs at their surfaces. The binding of antibodies to FcRs provides antigen-specificity to these cells, which upon activation release further cell-specific mediators of the immune response, such as interleukins, initiators of inflammation, leukotrienes, prostaglandins, histamines, or cytotoxic proteins. The adoptive specificity of the FcRs allows a combinatorial approach to pathogen elimination, by coupling the diversity of antibody antigen-recognition sites to the variety of cell-types expressing these receptors.

[0005] FcR-initiated mechanisms are important in normal immunity to infectious disease as well as in allergies, antibody-mediated tumor recognition, autoimmune diseases, and other diseases in which immune responses are abnormal (i.e., not regulated). Recent experiments with transgenic mice have demonstrated that the FcRs control key steps in the immune response, including antibody-directed cellular cytotoxicity and inflammatory cascades associated with the formation of immune complexes; see, for example, Ravetch et al., 1998, Annu Rev Immunolo 16, 421-432. Receptors that bind IgG (FcgRI, FcgRII, and FcgRIII, known collectively as FcgRs) mediate a variety of inflammatory reactions, regulate B-cell activation, and also trigger hypersensitivity reactions. The high affinity Fc epsilon receptor (also known as the IgE receptor or FceRI) is associated with the activation of mast cells and the triggering of allergic reactions and anaphylactic shock. Knockout mice for the FceRI alpha chain (FcεRIα) are unable to mount IgE-mediated anaphylaxis (see for example, Dombrowicz et al., 1993, Cell 75, 969-976), although FcgRs are still able to activate mast cells (see, for example, Dombrowicz et al., 1997, J. Clin. Invest. 99, 915-925; Oettgen et al., 1994, Nature 370, 367-370). FceRI has also been shown to trigger anti-parasitic reactions from platelets and eosinophils as well as deliver antigen into the MHC class II presentation pathway for the activation of T cells; see, for example, Gounni et al., 1994, Nature 367, 183-186; Joseph et al., 1997, Eur. J. Immunol. 27, 2212-2218; Maurer et al., 1998, J. Immunol. 161, 2731-2739. The beta subunit of FceRI has been associated with asthma in genetic studies; see, for example, Hill et al., 1996, Hum. Mol. Genet. 5, 959-962; Hill et al., 1995, Bmj 311, 776-779; Kim et al., 1998, Curr. Opin. Pulm. Med. 4, 46-48; Mao et al., 1998, Clin. Genet. 53, 54-56; Shirakawa et al., 1994, Nat. Genet. 7, 125-129. A significant fraction of the population (˜20%) may be affected by allergies, and this century has seen a substantial increase in asthma. Since IgE binding to FceRI is a requisite event in the reaction to different allergens, therapeutic strategies aimed at inhibiting FceRI could provide a useful treatment for these diseases. For example, monoclonal antibodies that target IgE and block receptor binding have shown therapeutic potential; see, for example, Heusser et al., 1997, Curr. Opin. Immunol. 9, 805-813.

[0006] FceRI is found as a tetrameric (abg₂) or trimeric (ag₂) membrane bound receptor on the surface of mast cells, basophils, eosinophils, langerhans cells and platelets. The alpha chain, also referred to as FcεRIα, of FceRI binds IgE molecules with high affinity (K_(D) of about 10⁻⁹ to 10⁻¹⁰ moles/liter (M)), and can be secreted as a 172-amino acid soluble, IgE-binding fragment by the introduction of a stop codon before the single C-terminal transmembrane anchor; see, for example, Blank et al.,1991,E. J. Biol. Chem. 266, 2639-2646, which describes the secretion of a soluble IgE-binding fragment of 172 amino acids. The extracellular domains of the human FcεRIα protein belong to the immunoglobulin (Ig) superfamily and contain seven N-linked glycosylation sites. Glycosylation of FcεRIα affects the secretion and stability of the receptor, but is not required for IgE-binding; see, for example, LaCroix et al., 1993, Mol. Immunol. 30, 321-330; Letoumeur et al.,1995, J. Biol. Chem. 270, 8249-8256; Robertson, 1993, J. Biol. Chem. 268, 12736-12743; Scarselli et al., 1993, FEBS Lett 329, 223-226. The beta and gamma chains of FceRI are signal transduction modules.

[0007] Prior investigators have disclosed the nucleic acid sequence for human FcεRIα; see, for example, U.S. Pat. No. 4,962,035, by Leder, issued Oct. 9, 1990; U.S. Pat. No. 5,639,660, by Kinet et al., issued Jun, 17, 1997; Kochan et al., 1988, Nucleic Acids Res. 16, 3584; Shimizu et al., 1988, Proc. Natl. Acad. Sci. USA 85, 1907-1911; and Pang et al., 1993, J. Immunol. 151, 6166-6174. Nucleic acid sequences have also been reported for the human FceRI beta and gamma chains; see, respectively, Kuster et al., 1992, J. Biol. Chem. 267, 12782-12787; Kuster et al., 1990, J. Biol. Chem. 265, 6448-6452. Nucleic acid sequences have also been reported for nucleic acid molecules encoding canine FcεRIα, murine FcεRIα, rat FcεRIα, feline FcεRIα and equine FcεRIα proteins; see, respectively, GenBank™ accession number D16413; Swiss-Prot accession number P20489 (represents encoded protein sequence); GenBank accession number J03606; PCT Publication No. WO 98/27208, by Frank et al., published Jun. 25, 1998, referred to herein as WO 98/27208; and PCT Publication No. WO 99/38974, by Weber et al., published Aug. 5, 1999, referred to herein as WO 99/38974. In addition, methods to detect IgE antibodies using a FcεRIα protein have been reported in PCT Publication No. WO 98/23964, by Frank et al., published Jun. 4, 1998, referred to herein as WO 98/23964; WO 98/27208, ibid.; PCT Publication No. WO 98/45707, by Frank et al., published Oct. 15, 1998, referred to herein as WO 98/45707; and WO 99/38974, ibid.. WO 98/23964, WO 98/27208, WO 98/45707 and WO 99/38974 are each incorporated by reference herein in its entirety.

[0008] There have been several reports of the use of mutagenesis and swapping techniques to attempt to identify amino acids of either FcεRIα or IgE involved in the binding of (i.e., interaction between) those respective proteins, reports attempting to model FcεRIα proteins based on homology to other Ig-superfamily members, and reports that identify compounds that apparently inhibit such binding; see, for example, Cook et al., 1997, Biochemistry 36, 15579-15588; Hulett et al., 1994, J. Biol. Chem. 269, 15287-15293; Hulett et al., 1995, J. Biol. Chem 270, 21188-21194; Mallamaci et al., 1993, J. Biol. Chem. 268, 22076-22083; Robertson, 1993, ibid.; Scarselli et al., 1993, ibid. McDonnell et al., 1997, Biochem. Soc. Trans. 25, 387-392; McDonnell et al., 1996, Nat. Struc. Biol. 3, 419-426; PCT Publication No. WO 97/40033, by Cheng et al., published Oct. 30, 1997; U.S. Pat. No. 5,180,805, by Gould et al, issued Jan. 19, 1993; U.S. Pat. No. 5,693,758, by Gould et al., issued Dec. 2, 1997; PCT Publication No. WO 96/01643, by Gould et al., published Jan. 25, 1996; PCT Publication No. WO 95/14779, by Gould et al., published Jun. 1, 1995. None of these references, however, describe isolated crystals of FcεRIα proteins or 3-D models derived from crystals.

[0009] Despite what is known about FcRs and their interaction with antibodies, there remains a need for FcRs and antibodies with improved characteristics, such as enhanced affinity for their ligands, altered substrate specificity, increased stability, and increased solubility for use in diagnosis, treatment and prevention of allergy and other abnormal immune responses. Also needed for safe and efficacious compounds to prevent or treat allergy and to regulate other immune responses in an animal.

SUMMARY OF THE INVENTION

[0010] The present invention includes an isolated crystal of a constant region (Fc region) of an antibody, a three-dimensional (3-D) model of such a crystal and a modification of such a model. The present invention also includes compounds that inhibit the ability of FcRs to bind to antibodies as well as antibody muteins and other modified antibodies. Also included in the present invention are methods to produce and use such crystals, models, inhibitory compounds, muteins, and other modified proteins. As such, the present invention includes antibodies with improved functions such as increased stability, increased affinity for an Ig binding domain of a FcR, altered substrate specificity, and increased solubility, including but not limited to reduced aggregation. Such proteins, also referred to as muteins, are useful to detect allergy and other immune response abnormalities as well as to protect an animal from such abnormalities. The present invention also provides safe and efficacious inhibitory compounds to protect (e.g., prevent, treat, reduce the consequences of) an animal from allergy and to regulate other immune responses in an animal.

[0011] The present invention includes a 3-D model of a human IgE Fc region comprising Cε3 and Cε4 domains, wherein the model substantially represents the atomic coordinates specified in Table 1, Table 2 or Table 3. The present invention also includes a 3-D model comprising a modification of a model substantially representing the atomic coordinates specified in Table 1, Table 2 or Table 3. Also included in the present invention are methods to produce such models.

[0012] The present invention also includes an isolated crystal of a human IgE Fc region comprising Cε3 and Cε4 domains.

[0013] The present invention includes a method to identify a compound that inhibits the binding between an IgE antibody and a FcεRIα protein. The method includes the step of using a 3-D model of the present invention, and particularly one substantially represents the atomic coordinates specified in Table 1, Table 2 or Table 3. Also included in the present invention are inhibitory compounds identified using such a method. Also included are therapeutic compositions that include such inhibitory compounds and methods to use such therapeutic compositions to protect an animal from allergy or to regulate other immune responses (e.g., protect an animal from other abnormal immune responses).

[0014] The present invention also includes a mutein that binds to a Fc binding domain of a FcR. Such a mutein has an improved function compared to a protein that includes SEQ ID NO:2. Examples of such an improved function include increased stability, increased affinity for an Fc domain of an antibody, altered substrate specificity, decreased aggregation, and increased solubility. Such a mutein is produced by a method that includes the following steps: (a) analyzing a 3-D model substantially representing the atomic coordinates specified in Table 1, Table 2, or Table 3 to identify at least one amino acid of the protein represented by the model which if replaced by a specified amino acid would effect an improved function of the protein; and (b) replacing the identified amino acid(s) to produce the mutein having such an improved function. The present invention also includes a mutein having an improved function compared to an unmodified IgE Fc region.

[0015] Also included are muteins that are chemically modified IgE Fc regions. Also included are nucleic acid molecules that encode muteins of the present invention, recombinant molecules and recombinant cells including such nucleic acid molecules and methods to produce such muteins. Also included are diagnostic reagents and diagnostic kits including such muteins, therapeutic compositions including such muteins, and methods to detect or protect an animal from allergy or other abnormal immune responses.

[0016] The present invention also includes a method to improve a function of a IgE Fc region which includes the steps of: (a) analyzing a 3-D model substantially representing the atomic coordinates specified in Table 1, Table 2 or Table 3 to identify at least one amino acid of the protein which if replaced by a specified amino acid improves at least one of the functions of the protein; and (b) replacing the identified amino acid(s) to produce a mutein having at least one of the improved functions.

BRIEF DESCRIPTION OF DRAWINGS

[0017]FIG. 1 shows a side-view comparison of the unbound IgE-Fc, receptor-bound IgE-Fc and IgG-Fc structures. The N-terminal domains are shown in blue. FIG. 1a shows the closed form of IgE-Fc Cε3-Cε4 domains. FIG. 1b shows the open form of IgE-Fc Cε3-Cε4 domains. FIG. 1c shows unbound IgG-Fc.

[0018]FIG. 2 is a top-view comparison of the unbound IgE-Fc, receptor-bound IgE-Fc and IgG-Fc structures (N-terminal domains). β-strands are labeled (A-G) and a line is drawn between the first residue of the A strands for each Fc structure. In the closed IgE confirmation, this distance is 13 Å, in the open form it is 23 Å and in the IgG-Fc structure it is 22 Å. FIG. 2a shows the closed form of IgE-Fc Cε3-Cε4 domains. FIG. 2b shows the open form of IgE-Fc Cε3-Cε4 domains. FIG. 2c shows unbound IgG-Fc.

[0019]FIG. 3 shows a superposition of nine crystallographically independent IgG-Fc structures (grey/blue) with the open (dark blue) and closed (red) IgE-Fc structures. The IgG and IgE Fc structures were superimposed using Cα carbons from the C-terminal domain (Cγ2 or Cε3). IgG-Fc structures were used from the PDB files 1IGT, 1FC1, 1FC2, 1FCC, 1IGY and 1ADQ. The 1MCO hinge-deleted antibody structure was not included in this analysis since it exhibits anomalous domain pairing throughout the protein structure. An asterisk is placed next to residue 366 in the BC loop of the IgE-Fc.

[0020]FIG. 4a shows a DynDom analysis of the domain motions characterizing the structural differences between bound and free IgE-Fc. One-half of an Fc (c3/c4 monomer) is shown in the closed conformation with the axis of the bend indicated by the dark red line. DynDom was used to determine the location of the axis and to calculate the change in the angle. Hinge residues (343-345, 351-352, and 435-436) are outlined in light purple. Residues that remain relatively fixed in both the open and closed forms of the Fc include the entire Cε4 domain, the interdomain linker, and the AB helix of Cε3. Residues in the Cε3 domain move as a semi-rigid domain. FIG. 4b shows a closeup of the residues at the Cε3/Cε4 and Cγ2/Cγ3 interfaces. IgG-Fc (red)(from pdb files 1IGT) and the closed IgE-Fc (blue) were superimposed using residues in the C-terminal domain (Cγ3 or Cε4). Note the displacement of the IgE-Fc helix (blue cylinder) away from the interdomain interface and the close approach of Cε3 residues to the IgG-Fc helix. The interactions of the AB helix with both domains may determine the full range of mobility of different antibody Fc domains. FIG. 4c shows a graph of the residue displacements observed for both chains of the IgE-Fc in the free and receptor-bound crystal structures. One chain is shown with red circles, the other with blue diamonds. The Cα distances between amino acid residues in each structure was calculated after superposition of the two structures based on the alignment of the two Cε4 domains. Loops involved in binding receptor are indicated and highlighted in yellow and move by approximately 6-14 Å in the free form. “N” indicates Cε3 A strand residues, “C” is the carboxy terminus, “L” identifies the poorly ordered Cε4 AB loop, and “X” identifies a difference due to crystal contacts.

[0021]FIG. 5a shows a surface representation of the Cε3 and Cε4 domains (top-view) in the closed (left) and open (right) IgE-Fc structures. Receptor binding residues are shown in magenta and are from the Cε3 BC, DE and FG loops. FIG. 5b shows a side-view of the Cε3 and Cε4 domains described in FIG. 5a.

[0022]FIG. 6 illustrates potential roles for IgE conformational changes in receptor-binding and structure-based inhibitor design. Open forms of the IgE molecule can interact with the high-affinity receptor (FcεRI), as shown by the crystal structure of the complex. IgE also binds to a low-affinity receptor, which is a trimer of C-type lectin domains (FceRII). FceRII could potentially interact with the closed form of the IgE structure as shown in the upper left hand portion of the figure. The lectin domains are shown in blue while the IgE-Fc Cε3 domains are shown in yellow. Only two of the three lectin domains are thought to interact with the IgE. Three distinct classes of inhibitors of the IgE interaction are also shown on the left hand side of the figure. One class could bind to the open IgE and compete for FceRI-binding sites (competitive, lower left). Another class could bind to a region of IgE near the Ce3/Ce4 hinge and stabilize the closed form of IgE, thus inhibiting FceRI binding indirectly (allosteric inhibitor, center left). A third class of inhibitors could interact with FceRI-binding regions of the IgE, but stabilize a closed form of the IgE, acting as both a competitive and conformational inhibitor of FceRI binding (conformational inhibitor, center left).

[0023]FIG. 7a depicts the general structure of the IgG and IgE antibodies. Both antibodies contain two isotype-specific heavy chains and two light chains (H₂L₂). The Fab domains contain both heavy and light chain components while the Fc domains (shaded pink) are derived exclusively from the light chains. The IgE-Fc contains an extra domain pair (Cε2) compared to the IgG-Fc. The IgE Cε3-Cε4 domains are homologous to the IgG Cγ2-Cγ3 domains. FIG. 7b shows a structure-based sequence alignment of human IgE-Fc Cε3-Cε4 with the sequences of four IgG-Fc's for which crystal structure have been solved. IgE secondary structure is indicted using arrows for β-strands and ribbons for α-helices. Color bars indicate hinge residues (blue), FcεRi-binding loops (pink) and carbohydrate attachment sites (green dots). Within the sequence alignment, conserved residues are indicated with light-blue shading while structural differences (insertions, deletions, changes in secondary structure) between the IgG and IgE are highlighted in yellow. In addition, the completely conserved Cγ2 AB helix histidine residue (H310 in Igg1, H329 in IgG2a) and the corresponding residue in IgE, threonine 409, are indicated in yellow and pink respectively. The IgE numbering (above the sequence) is according to Dorrington and Bennich. The numbering of human IgG1 is given directly below the sequence. The PDB numbering of murine IG2a (1IGT), is shown in italics at the bottom (note that there are deletions in this numbering system).

[0024]FIG. 8a shows a side-view comparison of the unbound IgE-Fc, receptor-bound IgE-Fc and IgG-Fc structures. The N-terminal domains are shown in blue. FIG. 8b is a top-view comparison of the unbound IgE-Fc, receptor-bound IgE-Fc and IgG-Fc structures (N-terminal domains). β-strands are labeled (A-G) and a line is drawn between the first residue of the A strands for each Fc structure. In the closed IgE confirmation, this distance is 13 Å, in the open form it is 23 Å and in the IgG-Fc structure it is 22 Å.

[0025]FIG. 9a shows a superposition of nine crystallographically independent IgG-Fc structures (grey/blue) with the open (dark blue) and closed (red) IgE-Fc structures. The IgG and IgE Fc structures were superimposed using Cα carbons from the C-terminal domain (Cγ2 or Cε3). IgG-Fc structures were used from the PDB files 1IGT, 1FC1, 1 FC2, 1FCC, 1IGY and 1ADQ. An asterisk is placed next to residue 366 in the BC loop of the IgE-Fc. Note the displacement of the IgE-Fc helix away from the interdomain interface, the movement of the IgE-Fc EF helix in the closed conformation, and the close approach of the IgG-Fc AB and EF helices at the site of the IgG residue insertion. FIG. 9b shows a DymDom analysis of the IgG-Fc. A stereo view of one chain of the Fc (closed conformation) is shown with the rotation axis indicated by an arrow. Hinge residues (343-345, 351-352, and 435-436) are outlined in cyan. Cε3 domain residues that move as a semi-rigid domain are shown in red. Residues that remain relatively fixed in both the open and closed forms of the Fc are shown in blue. FIG. 9c shows a DynDom analysis of three IgG-Fc structures. Shown is a stereo view with the rotation axes and hinge residues for murine IgG1 (1IGY) (cyan), murine IgG2a (1IGT) (purple) and human IgG1 (1FC1) (pink) on the Cα trace of the IgG2a structure. FIG. 9d shows the change in Cα coordinates between the closed and open conformations of the IgE-Fc. One chain is shown with red circles, the other with blue diamonds. Receptor binding loops are indicated and highlighted in pink; hinge residues are shown in cyan. “N” indicates Cε3 A strand residues, “C” is the carboxy terminus, “L” identifies the poorly ordered Cε4 AB loop, and “X” identifies a difference due to crystal contacts.

[0026]FIG. 10a diagrams the contacts made by the AB helix residues 9IgE Cε3 or IgG Cγ2). Residues of the AB and EF helices are shown on the grey helical wheels while the residues of the lower domain (Cε3 or Cε4) are shown below (blue lettering in blue ovals). Upper domain contacts (to Cε3 or Cγ2) involve residues in the EF helix and residues immediately adjacent to the AB helix. Lower domain contacts (to Cε4 or Cγ3) involve residues from the C, C′, F and G β-sheet strands and the FG loop. Contacts formed only in the open form of the IgE-Fc are indicated by dashed blue lines; the single contact formed only in the closed form is indicated by a red line. Contacts made by the conserved H329 in IgG are indicated by solid blue lines. The completely conserved EF helix H329 residue and the insertion residue I266 that forms a bulge just after the AB helix, are shown in yellow. FIG. 10b shows a surface representation of the interaction of EF helix residue T407 with the AB helix in the closed IgE-Fc while FIG. 10c shows this same interaction in the open IgE-Fc. FIG. 10d shows a surface representation of the packing interactions of the corresponding residue, the conserved h329, in IgG-Fc, with the bulge a the C-terminus of the Cγ2 AB helix.

[0027]FIG. 11a shows a molecular surface representation of the Cε3 and Cε4 domains (side-view) in the closed (left) and open (right) IgE-Fc structures. Receptor binding residues are shown in magenta and are from the Cε3 BC, DE and FG loops. FIG. 11b shows a top-view of the Cε3 and Cε4 domains described in FIG. 11a.

[0028]FIG. 12 shows possible roles for IgE flexibility in Fc receptor binding and structure-based inhibitor design. The Cε3 domains are colored to correspond to the different conformational states, open (pink) and closed (yellow); the Cε4 domains are shown in grey. Open forms of the IgE molecule can bind to the high affinity receptor, FcεRI. The low affinity receptor, FcεRII, is a trimeric C-type lectin that binds to an unidentified conformation of the IgE-Fc (green). Three potential classes of inhibitors of the IgE:FcεRI interactions are shown: binding site competitive inhibitor, binding sire conformational inhibitor, and allosteric conformational inhibitor.

[0029]FIG. 13 illustrates a potential drug binding site near the IgE-Fc hinge. A hypothetical drug (green) is shown inside the hinge cavity. Residues surrounding the cavity include R342, P343, S344, P3435, L348, W410, I411, K435, T436, R440,P471, E472, D473,E529.

DETAILED DESCRIPTION OF THE INVENTION

[0030] The present invention includes isolated crystals of Fc regions of antibodies, 3-D models of such crystals and modifications of such models. The present invention also includes compounds that inhibit the ability of FcRs to bind to antibodies as well as muteins and other modified antibodies. Also included in the present invention are methods to produce and use such crystals, models, inhibitory compounds, muteins, and other modified proteins.

[0031] The present invention includes an isolated crystal of a Fc region comprising the Cε3 and Cε4 domains of an IgE antibody (Fc-Cε3/Cε4), a 3-D model of such a crystal and a modification of such a model. As used herein, the term “a” entity or “an” entity refers to one or more of that entity; for example, a crystal or a model refers to one or more crystals or models, respectively. As such, the terms “a” (or “an”), “one or more” and “at least one” can be used interchangeably herein. It is also to be noted that the terms “comprising”, “including”, and “having” can be used interchangeably. Furthermore, a compound “selected from the group consisting of” refers to one or more of the compounds in the list that follows, including mixtures, or combinations, of two or more of the compounds.

[0032] As used herein, an extracellular domain of a FcεRIα protein is the portion of the FceRI alpha chain that is exposed to the environment outside the cell and that binds to the Fc domain of an IgE antibody. Such an extracellular domain can be (a) a complete extracellular domain which is a domain that extends from the first amino acid of a mature FceRI alpha chain through the last amino acid prior to the start of the transmembrane region or a domain that is functionally equivalent, in that such a domain includes a D1 and D2 domain, displays a similar affinity for the IgE antibody to which such an FcεRIα protein naturally binds, and produces crystals having sufficient quality to enable structure determination, or (b) a fragment of any of the extracellular domains of (a), wherein the fragment retains its ability to bind to the Fc domain of an antibody. As used herein, the terms binding to an antibody and binding to the Fc domain (i.e., constant region) of an antibody can be used interchangeably since it is recognized that a FcR binds to the Fc domain of an antibody. A FcR (i.e., a protein that can bind to an antibody), such as a FcεRIα protein, can be a full-length FcR (e.g., a full-length FceRI alpha chain), or any fragment thereof, wherein the fragment binds to an antibody. Similarly an antibody, or an Fc region thereof, can be a full-length antibody, or full-length Fc region thereof, or any fragment thereof that binds to a FcR. In one embodiment an Fc region comprises Cε3 and Cε4 domains. Preferably a FcR binds to an antibody with an affinity (K_(A)) of at least about 10⁸ liters/mole (M⁻¹), more preferably of at least about 10⁹ M⁻¹, and even more preferably of at least about 10¹⁰ M⁻¹.

[0033] The present invention is surprising in several aspects. For example, this is the first report of an isolated crystal of a Fc-Cε3/Cε4 region of an IgE antibody, and in particular of an isolated crystal of sufficient quality that a crystal structure, i.e., a 3-D model, could be derived therefrom. Generation of such a crystal was very difficult and non-obvious and has been attempted by others without success. The inventors tried many approaches before discovering a preferred Fc-Cε3/Cε4 region from which to make a useful crystal. The first such region to be used successfully is referred to herein as PhFc-Cε3/Cε4₁₋₂₂₂ which is composed of the four amino acids alanine, aspartic acid, proline and cysteine at the amino terminus followed by amino acids 330 through 547 of the human IgE Fc constant region, using the numbering system of Dorrington et al, 1978, Immunol Rev 41, 3-25. PhFc-Cε3/Cε4₁₋₂₂₂ is represented herein by SEQ ID NO:2. An example of a nucleic acid molecule encoding PhFc-Cε3/Cε4₁₋₂₂₂ is referred to herein as nhFc-Cε3/Cε4₁₋₆₆₆, the nucleic acid sequence of which is referred to herein as SEQ ID NO: 1. It was also discovered that better crystals are generated when PhFc-Cε3/Cε4₁₋₂₂₂ is produced in insect cells, using a method such as that described in the Examples. Solution of the crystal structure was also very difficult, as described in more detail in the Examples. For example, as part of the effort, approximately 12,000 models were generated and used in complete Molecular Replacement searches with the program Amore, taking about 10 days on 5 Silicon Graphics computers.

[0034] Determination of the crystal structure of PhFc-Cε3/Cε4₁₋₂₂₂ produced in Trichoplusia ni (Hi-5) cells resulted in a 3-D model that substantially represents the atomic coordinates specified in Table 1, Table 2 or Table 3. Amino acids are represented herein by their standard three or one letter codes; see, for example, Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Labs Press, 1989, which is incorporated herein by reference in its entirety.

[0035] The 3-D model of PhFc-Cε3/Cε4₁₋₂₂₂ is also very surprising in view of what is known about the crystal structure of the Fc region of IgG. The Fc region of IgE exists in a novel conformation that is more compact than that of IgG. The Cε3 domains are also much closer to each other in IgE compared to IgG (about 13 angstroms compared to about 22 angstroms), leading to the descriptor of “closed conformation” for the IgE Fc structure. This closed conformation is also surprising in view of the crystal structures of FcεRIα alone, which is disclosed in U.S. patent application Ser. No. 09/434,193, filed Nov. 4, 1999, by Jardetzky et al., and in PCT Publication No. WO 00/26246, published May 11, 2000, by Jardetzky et al., and of the complex between FcεRIα and Fc-Cε3/Cε4 alone, which is disclosed in U.S. patent application Ser. No. 60/189,853. U.S. Ser. No. 09/434,193, ibid., WO 00/26246, ibid. and 60/189,853, ibid., are incorporated by reference herein in their entireties. The structure of Fc-Cε3/Cε4 in the complex is an open conformation, also referred to as a receptor-bound conformation. The distance between the two Cε3 domains in the receptor-bound conformation is about 23 angstroms. Comparison of these structural similarities and differences are described in greater detail in the Examples and in Ser. No. 60/189,853, ibid. Analysis of the model which substantially represents the atomic coordinates specified in Table 1, Table 2 or Table 3 indicates the necessity of such a model for proper interpretation and refinement of mutagenesis studies that have been reported. Such a model permits differentiation between amino acids directly or indirectly influencing binding of FcεRIα to IgE and demonstrates where amino acids and amino acid segments identified in mutagenesis studies are positioned on the protein. By using a model of the present invention one can identify the interactions of FcεRIα and IgE, thereby identifying amino acids to target for mutein production or regions to target for the development of compounds to inhibit binding of IgE to its receptor. Such a model also leads to the ability to design inhibitory compounds that stabilize the closed conformation of IgE, thereby reducing its ability to bind to a FcR. Such a model can be used alone or in conjunction with a model of FcεRIα alone (U.S. Ser. No. 09/434,193, ibid. and WO 00/26246, ibid.) or of the complex between FcεRIα and Fc-Cε3/Cε4 alone (Ser. No. 60/189,853, ibid.).

[0036] One embodiment of the present invention is an isolated crystal of a Fc-Cε3/Cε4 region of an IgE antibody. As used herein, an isolated crystal is a crystal of a protein that has been produced in a laboratory; that is, an isolated crystal is produced by an individual and is not an object found in situ in nature. It is appreciated by those skilled in the art that there are a variety of techniques to produce crystals including, but not limited to, vapor diffusion using a hanging or sitting drop methodology, vapor diffusion under oil, and batch methods; see, for example, Ducruix et al., eds., 1991, Crystallization of nucleic acids and proteins; A practical approach, Oxford University Press, and Wyckoff et al., eds., 1985, Methods in Enzymology 11, 49-185; each reference is incorporated by reference herein in its entirety. It is also to be appreciated that crystallization conditions can be adjusted depending on a protein's inherent characteristics as well as on a protein's concentration in a solution and that a variety of precipitants can be added to a protein solution in order to effect crystallization; such precipitants are known to those skilled in the art. In a preferred embodiment, a crystal of a Fc-Cε3/Cε4 region is produced in a solution by adding a precipitant such as polyethylene glycol (PEG) or PEG monomethylether. It is also to be noted that a Fc-Cε3/CCε4 region used to produce a crystal can be produced by a variety of methods, including purification of a native protein, chemical synthesis of a protein, or recombinant production of a protein. Although a number of cell types can be used to recombinantly produce such a protein, insect cells, such as, but not limited to Trichoplusia ni and Spodoptera frugiperda, are preferred, with Trichoplusia ni cells being more preferred. Additional methods to produce proteins are disclosed below.

[0037] Isolated crystals of the present invention can include heavy atom derivatives, such as, but not limited to, gold, platinum, mercury, selenium, copper, and lead. Such heavy atoms can be introduced randomly or introduced in a manner based on knowledge of 3-D models of the present invention. Additional crystals of the present invention are not derivatized. In one embodiment, an isolated crystal of the present invention is a co-crystal of a FcεRIα protein bound to a Fc domain of an IgE antibody in the presence of a compound that inhibits the binding of a FcεRIα protein to a Fc domain of an IgE antibody. Additional crystals of the present invention include crystals produced from proteins that are muteins of the present invention or other proteins that are represented by a 3-D model of the present invention.

[0038] An isolated crystal of the present invention can be the crystal of any suitable Fc region that binds to FcεRIα, such as a Fc comprising Cε3 domains or a Fc comprising Cε3 and Cε4 domains. Suitable Fc-Cε3/Cε4 regions include mammalian Fc-Cε3/Cε4 regions, with human, canine, feline, equine, rat and murine Fc-Cε3/Cε4 regions being preferred, and human Fc-Cε3/Cε4 regions being even more preferred. A preferred crystal of the present invention diffracts X-rays to a resolution of about 4.5 angstroms or higher (i.e., lower number meaning higher resolution), with resolutions of about 4.0 angstroms or higher, about 3.5 angstroms or higher, about 3.25 angstroms or higher, about 3 angstroms or higher, about 2.5 angstroms or higher, about 2.3 angstroms or higher, about 2 angstroms or higher, about 1.5 angstroms or higher, and about 1 angstrom or higher being increasingly more preferred. It is appreciated, however, that additional crystals of lower resolutions can have utility in discerning overall topology of the structures, e.g., location of a binding site or where a molecule binds to a receptor or to an antibody. A particularly preferred isolated crystal of the present invention has amino acid sequence SEQ ID NO:2, or a sequence essentially equivalent that represents another mammalian Fc-Cε3/Cε4 region. Preferred are crystals that belong to spacegroup P42₁2. Particularly preferred crystals include a crystal belonging to spacegroup P42₁2 that has cell dimensions of 105.6 angstroms×105.6 angstroms×47.1 angstroms, alpha=beta=gamma=90 degrees and that contains one Cε3/Cε4 chain per asymmetric unit of the crystal. Such a preferred crystal preferably diffracts X-rays to a resolution of about 2.3 angstroms.

[0039] The present invention includes a 3-D model of a Fc-Cε3/Cε4 region that substantially represents the atomic coordinates specified in Table 1, Table 2 or Table 3. The present invention also includes 3-D models that comprise modifications of the model substantially represented by the atomic coordinates specified in Table 1, Table 2 or Table 3. Each such modification represents an antibody Fc region that binds to a Fc receptor protein. A 3-D model of a Fc-Cε3/Cε4 region is a representation, or image, that predicts the actual structure of the corresponding region. As such, a 3-D model is a tool that can be used to probe the relationship between the region's structure and function at the atomic level and to design muteins (i.e., genetically and/or chemically altered antibodies) having an improved function, such as, but not limited to: increased (i.e., enhanced) stability; increased FcR binding activity, for example, by, increasing the affinity for an FcR by, for example, increasing the association rate and/or decreasing the dissociation rate between a FcR and an antibody or by altering substrate specificity (e.g., enhancing the ability of an Fc region of a certain species and class to bind to an antibody binding site from another species and/or another antibody class); and/or increased solubility (e.g., reduced aggregation). It is well known to those skilled in the art, however, that a 3-D model of a protein derived by analysis of protein crystals is not identical to the inherent structure of the protein. See, for example, Branden et al., Introduction to Protein Structure, Garland Publishing Inc., New York and London, 1991, especially on page 277, which states “not surprisingly the model never corresponds precisely to the actual crystal.” Furthermore, the model can be subjected to further refinements to more closely correspond to the actual structure of a Fc region of an antibody. Such a refined model, which is an example of a modification of the present invention, is a better predictor of the actual structure and mechanism of action of the protein that the model represents. A refinement of a 3-D model of the present invention refers to an improved model of a Fc-Cε3/Cε4 region that can be obtained in a variety of ways known to those skilled in the art. Refinements can include models determined to more preferred degrees of resolution, preferably to about 4.5 angstroms, more preferably to about 4 angstroms, more preferably to about 3.5 angstroms, more preferably to about 3.25 angstroms, more preferably to about 3 angstroms, more preferably to about 2.5 angstroms, more preferably to about 2.3 angstroms, more preferably to about 2 angstroms, more preferably to about 1.5 angstroms, and even more preferably to about 1 angstrom. Preferred refinements are obtained using the 3-D model as a basis for such improvements.

[0040] One embodiment of the present invention is a 3-D model of a Fc-Cε3/Cε4 region that substantially represents the atomic coordinates specified (i.e., listed) in Table 1. TABLE 1 Atomic coordinates of 7_more_dimer.pdb ATOM ATOM # TYPE RES CHN # X Y Z OCC B 1 CB VAL A 336 46.217 60.546 16.604 1.00 63.58 2 CG1 VAL A 336 45.590 59.856 15.405 1.00 64.78 3 CG2 VAL A 336 47.677 60.888 16.335 1.00 68.51 4 C VAL A 336 44.045 61.436 17.434 1.00 61.62 5 O VAL A 336 43.880 60.399 18.074 1.00 64.02 6 N VAL A 336 46.161 62.624 17.972 1.00 59.58 7 CA VAL A 336 45.438 61.827 16.943 1.00 61.95 8 N SER A 337 43.046 62.262 17.137 1.00 59.54 9 CA SER A 337 41.679 61.982 17.564 1.00 57.94 10 CB SER A 337 41.204 63.069 18.525 1.00 56.70 11 OG SER A 337 41.581 64.347 18.053 1.00 65.28 12 C SER A 337 40.697 61.833 16.400 1.00 56.67 13 O SER A 337 40.987 62.234 15.268 1.00 56.61 14 N ALA A 338 39.539 61.245 16.687 1.00 52.92 15 CA ALA A 338 38.521 61.011 15.671 1.00 51.01 16 CB ALA A 338 38.576 59.562 15.216 1.00 50.96 17 C ALA A 338 37.120 61.348 16.166 1.00 50.95 18 O ALA A 338 36.816 61.204 17.352 1.00 53.16 19 N TYR A 339 36.272 61.805 15.250 1.00 47.68 20 CA TYR A 339 34.903 62.169 15.592 1.00 48.08 21 CB TYR A 339 34.810 63.675 15.897 1.00 50.34 22 CC TYR A 339 35.892 64.218 16.817 1.00 58.74 23 CD1 TYR A 339 37.196 64.421 16.355 1.00 60.22 24 CE1 TYR A 339 38.199 64.895 17.205 1.00 64.78 25 CD2 TYR A 339 35.616 64.506 18.153 1.00 60.49 26 CE2 TYR A 339 36.608 64.980 19.012 1.00 63.00 27 CZ TYR A 339 37.900 65.172 18.533 1.00 67.92 28 OH TYR A 339 38.891 65.626 19.382 1.00 68.47 29 C TYR A 339 33.954 61.815 14.437 1.00 45.49 30 O TYR A 339 34.262 62.044 13.267 1.00 43.52 31 N LEU A 340 32.808 61.238 14.775 1.00 44.01 32 CA LEU A 340 31.816 60.872 13.776 1.00 42.54 33 CB LEU A 340 31.550 59.363 13.816 1.00 39.07 34 CG LEU A 340 30.652 58.750 12.730 1.00 39.58 35 CD1 LEU A 340 31.198 59.074 11.349 1.00 28.76 36 CD2 LEU A 340 30.571 57.236 12.923 1.00 35.57 37 C LEU A 340 30.557 61.645 14.134 1.00 42.53 38 O LEU A 340 30.138 61.638 15.286 1.00 43.25 39 N SER A 341 29.957 62.324 13.160 1.00 42.42 40 CA SER A 341 28.752 63.103 13.425 1.00 40.32 41 CB SER A 341 28.997 64.586 13.105 1.00 41.30 42 OG SER A 341 29.416 64.758 11.764 1.00 45.86 43 C SER A 341 27.563 62.606 12.634 1.00 38.67 44 O SER A 341 27.707 62.048 11.559 1.00 42.94 45 N ARC A 342 26.378 62.823 13.177 1.00 37.60 46 CA ARC A 342 25.155 62.414 12.520 1.00 35.91 47 CB ARG A 342 24.026 62.359 13.552 1.00 36.67 48 CG ARG A 342 24.254 61.315 14.646 1.00 39.89 49 CD ARG A 342 23.141 61.322 15.679 1.00 42.31 50 NE ARG A 342 23.185 62.534 16.490 1.00 45.87 51 CZ ARC A 342 24.005 62.730 17.520 1.00 52.30 52 NH1 ARG A 342 24.861 61.790 17.895 1.00 56.74 53 NH2 ARG A 342 23.981 63.885 18.168 1.00 58.22 54 C ARC A 342 24.832 63.409 11.398 1.00 34.19 55 O ARC A 342 25.476 64.450 11.278 1.00 34.44 56 N PRO A 343 23.837 63.101 10.555 1.00 31.22 57 CD PRO A 343 23.028 61.871 10.494 1.00 34.08 58 CA PRO A 343 23.486 64.024 9.466 1.00 33.86 59 CE PRO A 343 22.437 63.244 8.663 1.00 32.10 60 CO PRO A 343 22.698 61.789 9.022 1.00 37.07 61 C PRO A 343 22.897 65.323 10.015 1.00 32.54 62 O PRO A 343 22.270 65.319 11.072 1.00 35.02 63 N SER A 344 23.090 66.432 9.311 1.00 33.04 64 CA SER A 344 22.515 67.687 9.778 1.00 34.74 65 CE SER A 344 23.172 68.897 9.095 1.00 35.18 66 OG SER A 344 22.663 69.093 7.792 1.00 35.70 67 C SER A 344 21.038 67.628 9.415 1.00 35.17 68 O SER A 344 20.669 67.132 8.349 1.00 32.53 69 N PRO A 345 20.162 68.094 10.313 1.00 35.98 70 CD PRO A 345 20.377 68.420 11.736 1.00 36.93 71 CA PRO A 345 18.731 68.056 9.995 1.00 34.79 72 CE PRO A 345 18.097 68.730 11.212 1.00 30.45 73 CG PRO A 345 18.988 68.221 12.331 1.00 30.91 74 C PRO A 345 18.385 68.739 8.667 1.00 34.13 75 O PRO A 345 17.471 68.317 7.963 1.00 34.14 76 N PHE A 346 19.124 69.783 8.309 1.00 31.57 77 CA PHE A 346 18.848 70.466 7.059 1.00 33.19 78 CB PHE A 346 19.711 71.724 6.935 1.00 37.49 79 CG PHE A 346 19.616 72.394 5.595 1.00 38.65 80 CO1 PHE A 346 18.432 72.979 5.178 1.00 42.62 81 CD2 PHE A 346 20.719 72.441 4.747 1.00 43.21 82 CE1 PHE A 346 18.344 73.608 3.933 1.00 41.72 83 CE2 PHE A 346 20.643 73.069 3.496 1.00 49.00 84 CZ PHE A 346 19.452 73.654 3.091 1.00 42.82 85 C PHE A 346 19.099 69.530 5.867 1.00 33.37 86 O PHE A 346 18.284 69.457 4.948 1.00 33.52 87 N ASP A 347 20.216 68.810 5.884 1.00 32.94 88 CA ASP A 347 20.533 67.891 4.792 1.00 33.61 89 CE ASP A 347 21.962 67.358 4.927 1.00 29.68 90 CG ASP A 347 23.011 68.378 4.541 1.00 35.85 91 OD1 ASP A 347 24.214 68.084 4.718 1.00 42.71 92 OD2 ASP A 347 22.646 69.472 4.056 1.00 50.58 93 C ASP A 347 19.564 66.718 4.762 1.00 33.62 94 O ASP A 347 19.201 66.219 3.699 1.00 30.10 95 N LEU A 348 19.137 66.288 5.940 1.00 34.23 96 CA LEU A 348 18.226 65.163 6.054 1.00 38.75 97 CE LEU A 348 18.260 64.636 7.496 1.00 38.06 98 CG LEU A 348 17.363 63.435 7.811 1.00 43.84 99 CD1 LEU A 348 17.739 62.243 6.910 1.00 39.77 100 CD2 LEU A 348 17.510 63.064 9.291 1.00 43.35 101 C LEU A 348 16.763 65.439 5.645 1.00 39.57 102 O LEU A 348 16.146 64.621 4.959 1.00 38.51 103 N PHE A 349 16.214 66.583 6.057 1.00 40.41 104 CA PHE A 349 14.809 66.901 5.762 1.00 42.87 105 CB PHE A 349 14.111 67.364 7.040 1.00 39.59 106 CG PHE A 349 14.208 66.383 8.163 1.00 37.95 107 CD1 PHE A 349 15.004 66.649 9.268 1.00 36.40 108 CD2 PHE A 349 13.517 65.181 8.105 1.00 40.49 109 CE1 PHE A 349 15.116 65.726 10.305 1.00 39.63 110 CE2 PHE A 349 13.619 64.247 9.135 1.00 38.12 111 CZ PHE A 349 14.418 64.520 10.237 1.00 41.86 112 C PHE A 349 14.472 67.896 4.654 1.00 44.67 113 O PHE A 349 13.433 67.773 4.001 1.00 47.25 114 N ILE A 350 15.314 68.895 4.450 1.00 46.06 115 CA ILE A 350 15.027 69.871 3.417 1.00 50.35 116 CB ILE A 350 15.548 71.270 3.813 1.00 50.30 117 CG2 ILE A 350 14.997 72.316 2.864 1.00 51.91 118 CG1 ILE A 350 15.146 71.593 5.261 1.00 51.78 119 CD1 ILE A 350 13.685 71.366 5.580 1.00 45.73 120 C ILE A 350 15.694 69.421 2.127 1.00 51.95 121 O ILE A 350 15.028 69.146 1.130 1.00 52.71 122 N ARG A 351 17.016 69.319 2.173 1.00 53.39 123 CA ARG A 351 17.813 68.909 1.031 1.00 54.67 124 CB ARG A 351 19.290 69.059 1.393 1.00 59.14 125 CO ARG A 351 20.186 69.537 0.267 1.00 64.87 126 CD ARG A 351 21.254 70.473 0.808 1.00 66.51 127 NE ARG A 351 22.405 70.566 −0.080 1.00 73.42 128 CZ ARG A 351 23.263 69.573 −0.283 1.00 78.26 129 NH1 ARG A 351 23.094 68.417 0.344 1.00 81.30 130 NH2 ARG A 351 24.288 69.733 −1.111 1.00 79.63 131 C ARG A 351 17.508 67.468 0.616 1.00 53.92 132 O ARG A 351 17.510 67.144 −0.567 1.00 53.66 133 N LYS A 352 17.248 66.612 1.598 1.00 53.41 134 CA LYE A 352 16.942 65.200 1.360 1.00 53.02 135 CE LYS A 352 15.779 65.053 0.375 1.00 54.25 136 CG LYS A 352 14.506 65.752 0.814 1.00 64.61 137 CD LYS A 352 13.366 65.442 −0.146 1.00 71.92 138 CE LYE A 352 12.202 66.410 0.014 1.00 76.75 139 NZ LYS A 352 12.573 67.793 −0.405 1.00 82.42 140 C LYE A 352 18.130 64.383 0.847 1.00 51.14 141 O LYS A 352 17.945 63.417 0.109 1.00 51.55 142 N SER A 353 19.341 64.772 1.237 1.00 47.69 143 CA SER A 353 20.552 64.067 0.832 1.00 45.50 144 CE SER A 353 21.154 64.718 −0.418 1.00 50.28 145 OG SER A 353 21.538 66.058 −0.171 1.00 63.45 146 C SER A 353 21.528 64.135 2.006 1.00 40.39 147 O SER A 353 22.498 64.890 1.995 1.00 40.20 148 N PRO A 354 21.268 63.329 3.045 1.00 36.74 149 CD PRO A 354 20.188 62.338 3.039 1.00 36.52 150 CA PRO A 354 22.043 63.224 4.283 1.00 34.20 151 CB PRO A 354 21.182 62.317 5.163 1.00 31.70 152 CO PRO A 354 19.870 62.260 4.472 1.00 40.26 153 C PRO A 354 23.433 62.636 4.121 1.00 32.13 154 O PRO A 354 23.655 61.771 3.283 1.00 28.54 155 N THR A 355 24.359 63.111 4.942 1.00 30.96 156 CA THR A 355 25.718 62.601 4.936 1.00 31.86 157 CB THR A 355 26.692 63.501 4.121 1.00 32.67 158 OG1 THR A 355 26.806 64.777 4.752 1.00 34.86 159 CG2 THR A 355 26.194 63.706 2.699 1.00 34.90 160 C THR A 355 26.221 62.548 6.374 1.00 33.38 161 O THR A 355 25.703 63.239 7.260 1.00 32.61 162 N ILE A 356 27.197 61.691 6.618 1.00 32.83 163 CA ILE A 356 27.793 61.641 7.935 1.00 33.21 164 CB ILE A 356 27.538 60.303 8.666 1.00 34.88 165 CG2 ILE A 356 26.038 60.142 8.910 1.00 34.84 166 CG1 ILE A 356 28.098 59.135 7.860 1.00 37.26 167 CD1 ILE A 356 27.809 57.757 8.489 1.00 38.06 168 C ILE A 356 29.265 61.855 7.639 1.00 32.48 169 O ILE A 356 29.739 61.563 6.536 1.00 30.30 170 N THR A 357 29.991 62.364 8.622 1.00 33.59 171 CA THR A 357 31.389 62.671 8.406 1.00 32.83 172 CB THR A 357 31.575 64.216 8.243 1.00 37.46 173 OG1 THR A 357 30.985 64.645 7.009 1.00 35.11 174 CG2 THR A 357 33.047 64.599 8.258 1.00 40.13 175 C THR A 357 32.274 62.180 9.530 1.00 34.22 176 O THR A 357 31.991 62.378 10.716 1.00 33.99 177 N CYS A 358 33.369 61.555 9.134 1.00 34.04 178 CA CYS A 358 34.344 61.037 10.068 1.00 36.90 179 C CYS A 358 35.496 62.027 9.999 1.00 36.26 180 O CYS A 358 36.103 62.188 8.944 1.00 35.68 181 CB CYS A 358 34.809 59.670 9.593 1.00 39.83 182 SG CYS A 358 35.781 58.719 10.798 1.00 52.73 183 N LEU A 359 35.780 62.692 11.112 1.00 38.57 184 CA LEU A 359 36.849 63.679 11.178 1.00 42.35 185 CB LEU A 359 36.327 64.985 11.796 1.00 42.11 186 CG LEU A 359 37.373 66.028 12.219 1.00 48.42 187 CD1 LEU A 359 38.221 66.454 11.027 1.00 49.46 188 CD2 LEU A 359 36.666 67.230 12.831 1.00 48.09 189 C LEU A 359 38.011 63.163 12.005 1.00 45.39 190 O LEU A 359 37.834 62.806 13.165 1.00 48.73 191 N VAL A 360 39.195 63.121 11.407 1.00 47.72 192 CA VAL A 360 40.395 62.669 12.104 1.00 51.87 193 CB VAL A 360 41.086 61.525 11.335 1.00 52.99 194 CG1 VAL A 360 42.365 61.110 12.049 1.00 51.29 195 CG2 VAL A 360 40.144 60.348 11.210 1.00 52.42 196 C VAL A 360 41.379 63.833 12.226 1.00 55.21 197 O VAL A 360 41.634 64.537 11.247 1.00 56.01 198 N VAL A 361 41.920 64.042 13.423 1.00 57.47 199 CA VAL A 361 42.882 65.121 13.652 1.00 61.75 200 CB VAL A 361 42.352 66.153 14.675 1.00 58.91 201 CG1 VAL A 361 43.389 67.232 14.913 1.00 56.98 202 CG2 VAL A 361 41.070 66.774 14.166 1.00 54.49 203 C VAL A 361 44.197 64.555 14.177 1.00 66.78 204 O VAL A 361 44.208 63.764 15.119 1.00 67.30 205 N ASP A 362 45.301 64.959 13.556 1.00 72.35 206 CA ASP A 362 46.631 64.500 13.955 1.00 79.16 207 CB ASP A 362 47.334 63.825 12.769 1.00 83.66 208 CG ASP A 362 48.603 63.089 13.176 1.00 87.40 209 OD1 ASP A 362 49.071 63.283 14.320 1.00 91.40 210 OD2 ASP A 362 49.138 62.318 12.348 1.00 87.33 211 C ASP A 362 47.444 65.704 14.424 1.00 82.84 212 O ASP A 362 47.937 66.487 13.607 1.00 84.14 213 N ALA A 363 47.578 65.849 15.740 1.00 85.70 214 CA ALA A 363 48.319 66.964 16.325 1.00 89.05 215 CB ALA A 363 48.446 66.770 17.830 1.00 90.18 216 C ALA A 363 49.701 67.142 15.699 1.00 91.80 217 O ALA A 363 50.243 68.246 15.691 1.00 92.23 218 N ALA A 364 50.263 66.056 15.174 1.00 94.23 219 CA ALA A 364 51.578 66.085 14.536 1.00 97.42 220 CB ALA A 364 52.668 66.159 15.594 1.00 96.05 221 C ALA A 364 51.755 64.828 13.687 1.00 100.00 222 O ALA A 364 51.767 63.715 14.213 1.00 101.29 223 N PRO A 365 51.885 64.988 12.359 1.00 101.76 224 CD PRO A 365 51.407 66.158 11.597 1.00 101.62 225 CA PRO A 365 52.053 63.836 11.468 1.00 103.14 226 CB PRO A 365 51.022 64.114 10.394 1.00 103.27 227 CG PRO A 365 51.228 65.594 10.183 1.00 103.12 228 C PRO A 365 53.456 63.681 10.872 1.00 104.03 229 O PRO A 365 54.419 63.372 11.579 1.00 104.47 230 N ALA A 366 53.536 63.884 9.557 1.00 104.37 231 CA ALA A 366 54.776 63.793 8.793 1.00 104.87 232 CB ALA A 366 55.839 64.705 9.413 1.00 105.36 233 C ALA A 366 55.319 62.370 8.665 1.00 104.90 234 O ALA A 366 56.461 62.108 9.045 1.00 105.14 235 N LYS A 367 54.514 61.452 8.129 1.00 104.05 236 CA LYS A 367 54.982 60.077 7.972 1.00 103.07 237 CB LYS A 367 55.483 59.539 9.315 1.00 103.33 238 CG LYS A 367 54.411 59.406 10.383 1.00 102.12 239 CD LYS A 367 54.951 58.638 11.572 1.00 103.99 240 CE LYS A 367 53.876 58.371 12.604 1.00 103.83 241 NZ LYS A 367 54.417 57.544 13.714 1.00 105.88 242 C LYS A 367 54.024 59.046 7.373 1.00 102.12 243 O LYS A 367 53.888 57.947 7.915 1.00 103.05 244 N GLY A 368 53.365 59.372 6.265 1.00 99.91 245 CA GLY A 368 52.480 58.388 5.664 1.00 96.70 246 C GLY A 368 51.079 58.800 5.255 1.00 94.03 247 O GLY A 368 50.829 59.949 4.891 1.00 94.76 248 N ALA A 369 50.162 57.839 5.313 1.00 90.44 249 CA ALA A 369 48.772 58.066 4.935 1.00 86.18 250 CB ALA A 369 48.460 57.308 3.645 1.00 86.97 251 C ALA A 369 47.808 57.639 6.038 1.00 82.79 252 O ALA A 369 48.149 56.827 6.897 1.00 83.46 253 N VAL A 370 46.600 58.193 6.001 1.00 78.82 254 CA VAL A 370 45.567 57.881 6.985 1.00 73.44 255 CB VAL A 370 45.161 59.132 7.777 1.00 71.37 256 CG1 VAL A 370 44.145 58.763 8.840 1.00 68.72 257 CG2 VAL A 370 46.388 59.769 8.404 1.00 66.32 258 C VAL A 370 44.347 57.346 6.252 1.00 71.19 259 O VAL A 370 43.803 58.019 5.383 1.00 70.77 260 N ASN A 371 43.913 56.138 6.605 1.00 69.11 261 CA ASN A 371 42.769 55.531 5.936 1.00 67.35 262 CB ASN A 371 43.145 54.138 5.430 1.00 68.95 263 CG ASN A 371 44.330 54.168 4.498 1.00 73.37 264 OD1 ASN A 371 44.299 54.828 3.459 1.00 76.52 265 ND2 ASN A 371 45.387 53.454 4.863 1.00 76.06 266 C ASN A 371 41.491 55.441 6.766 1.00 65.35 267 O ASN A 371 41.516 55.146 7.964 1.00 63.63 268 N LEU A 372 40.373 55.708 6.100 1.00 63.51 269 CA LEU A 372 39.060 55.651 6.721 1.00 60.50 270 CB LEU A 372 38.386 57.027 6.705 1.00 60.09 271 CG LEU A 372 39.139 58.170 7.386 1.00 61.37 272 CD1 LEU A 372 38.265 59.404 7.412 1.00 63.12 273 CD2 LEU A 372 39.517 57.771 8.791 1.00 62.53 274 C LEU A 372 38.220 54.658 5.936 1.00 57.54 275 O LEU A 372 38.069 54.776 4.720 1.00 58.06 276 N THR A 373 37.681 53.674 6.642 1.00 54.64 277 CA THR A 373 36.855 52.648 6.026 1.00 52.59 278 CB THR A 373 37.425 51.254 6.314 1.00 54.37 279 OG1 THR A 373 38.799 51.217 5.909 1.00 60.15 280 CG2 THR A 373 36.645 50.191 5.555 1.00 57.66 281 C THR A 373 35.444 52.722 6.591 1.00 48.12 282 O THR A 373 35.263 52.797 7.803 1.00 46.78 283 N TRP A 374 34.450 52.705 5.709 1.00 45.42 284 CA TRP A 374 33.057 52.767 6.129 1.00 44.33 285 CS TRP A 374 32.260 53.762 5.277 1.00 40.42 286 CG TRP A 374 32.664 55.183 5.442 1.00 41.22 287 CD2 TRP A 374 32.215 56.090 6.457 1.00 35.68 288 CE2 TRP A 374 32.841 57.329 6.219 1.00 31.67 289 CE3 TRP A 374 31.342 55.972 7.545 1.00 35.08 290 CD1 TRP A 374 33.523 55.888 4.652 1.00 38.77 291 NE1 TRP A 374 33.634 57.180 5.112 1.00 37.27 292 CZ2 TRP A 374 32.621 58.447 7.027 1.00 32.53 293 CZ3 TRP A 374 31.121 57.084 8.352 1.00 36.03 294 CH2 TRP A 374 31.760 58.304 8.087 1.00 33.34 295 C TRP A 374 32.385 51.405 6.022 1.00 44.84 296 O TRP A 374 32.758 50.581 5.186 1.00 43.54 297 N SER A 375 31.395 51.181 6.882 1.00 44.41 298 CA SER A 375 30.633 49.940 6.887 1.00 45.63 299 CB SER A 375 31.432 48.800 7.535 1.00 47.59 300 OG SER A 375 31.512 48.938 8.943 1.00 49.42 301 C SER A 375 29.308 50.112 7.618 1.00 45.23 302 O SER A 375 29.162 50.991 8.471 1.00 46.27 303 N ARG A 376 28.341 49.277 7.257 1.00 42.63 304 CA ARG A 376 27.033 49.307 7.882 1.00 41.96 305 CB ARG A 376 25.924 49.263 6.834 1.00 43.72 306 CG ARG A 376 25.855 50.458 5.901 1.00 40.62 307 CD ARG A 376 24.405 50.693 5.520 1.00 41.72 308 NE ARG A 376 24.143 50.468 4.110 1.00 52.53 309 CZ ARG A 376 22.929 50.305 3.599 1.00 52.81 310 NH1 ARG A 376 21.859 50.335 4.386 1.00 51.46 311 NH2 ARG A 376 22.781 50.128 2.293 1.00 56.61 312 C ARG A 376 26.920 48.082 8.775 1.00 39.96 313 O ARG A 376 27.218 46.971 8.355 1.00 40.84 314 N ALA A 377 26.503 48.285 10.014 1.00 41.64 315 CA ALA A 377 26.350 47.177 10.946 1.00 41.34 316 CB ALA A 377 25.705 47.680 12.227 1.00 33.50 317 C ALA A 377 25.502 46.056 10.325 1.00 41.22 318 O ALA A 377 25.685 44.888 10.648 1.00 41.04 319 N SER A 378 24.592 46.421 9.423 1.00 40.92 320 CA SER A 378 23.719 45.451 8.773 1.00 42.71 321 CB SER A 378 22.491 46.139 8.185 1.00 44.29 322 OG SER A 378 22.842 46.867 7.020 1.00 42.78 323 C SER A 378 24.420 44.706 7.658 1.00 43.58 324 O SER A 378 23.851 43.791 7.078 1.00 44.22 325 N GLY A 379 25.646 45.117 7.349 1.00 43.82 326 CA GLY A 379 26.409 44.463 6.304 1.00 45.23 327 C GLY A 379 26.060 44.917 4.901 1.00 48.43 328 O GLY A 379 26.747 44.562 3.943 1.00 47.67 329 N LYS A 380 24.995 45.699 4.763 1.00 50.04 330 CA LYS A 380 24.603 46.177 3.447 1.00 52.22 331 CB LYS A 380 23.238 46.868 3.509 1.00 54.82 332 CG LYS A 380 22.096 45.879 3.646 1.00 63.15 333 CD LYS A 380 20.734 46.528 3.466 1.00 70.67 334 CE LYS A 380 19.640 45.467 3.455 1.00 75.50 335 NZ LYS A 380 18.275 46.051 3.354 1.00 80.58 336 C LYS A 380 25.655 47.107 2.851 1.00 52.26 337 O LYS A 380 26.495 47.656 3.565 1.00 49.96 338 N PRO A 381 25.626 47.285 1.522 1.00 53.55 339 CD PRO A 381 24.694 46.657 0.571 1.00 54.43 340 CA PRO A 381 26.584 48.147 0.818 1.00 54.97 341 CB PRO A 381 26.212 47.948 −0.655 1.00 57.06 342 CG PRO A 381 25.519 46.611 −0.673 1.00 59.10 343 C PRO A 381 26.532 49.626 1.207 1.00 54.14 344 O PRO A 381 25.457 50.178 1.467 1.00 55.04 345 N VAL A 382 27.701 50.256 1.251 1.00 52.78 346 CA VAL A 382 27.801 51.680 1.546 1.00 53.97 347 CB VAL A 382 28.891 51.997 2.611 1.00 54.50 348 CG1 VAL A 382 28.595 51.252 3.896 1.00 56.74 349 CG2 VAL A 382 30.281 51.645 2.078 1.00 46.72 350 C VAL A 382 28.202 52.338 0.226 1.00 54.10 351 O VAL A 382 28.910 51.735 −0.583 1.00 53.38 352 N ASN A 383 27.752 53.566 0.011 1.00 53.55 353 CA ASN A 383 28.073 54.289 −1.210 1.00 54.35 354 CB ASN A 383 27.135 55.485 −1.370 1.00 60.43 355 CG ASN A 383 25.677 55.087 −1.371 1.00 67.43 356 OD1 ASN A 383 24.806 55.890 −1.037 1.00 75.26 357 ND2 ASN A 383 25.399 53.845 −1.756 1.00 72.99 358 C ASN A 383 29.520 54.779 −1.218 1.00 52.64 359 O ASN A 383 30.292 54.518 −0.293 1.00 50.26 360 N HIS A 384 29.879 55.493 −2.276 1.00 51.74 361 CA HIS A 384 31.225 56.038 −2.415 1.00 51.28 362 CB HIS A 384 31.499 56.380 −3.879 1.00 59.06 363 CG HIS A 384 31.657 55.179 −4.761 1.00 65.42 364 CD2 HIS A 384 30.912 54.727 −5.796 1.00 72.26 365 ND1 HIS A 384 32.694 54.284 −4.615 1.00 70.87 366 CE1 HIS A 384 32.581 53.330 −5.523 1.00 76.58 367 NE2 HIS A 384 31.507 53.576 −6.253 1.00 77.95 368 C HIS A 384 31.362 57.294 −1.555 1.00 47.99 369 O HIS A 384 30.478 58.145 −1.544 1.00 45.37 370 N SER A 385 32.473 57.413 −0.844 1.00 45.57 371 CA SER A 385 32.674 58.564 0.015 1.00 45.69 372 CB SER A 385 33.134 58.097 1.405 1.00 41.19 373 OG SER A 385 34.299 57.285 1.338 1.00 41.34 374 C SER A 385 33.654 59.598 −0.560 1.00 44.94 375 O SER A 385 34.413 59.313 −1.482 1.00 41.64 376 N THR A 386 33.603 60.805 −0.007 1.00 45.73 377 CA THR A 386 34.467 61.898 −0.421 1.00 46.08 378 CB THR A 386 33.670 63.191 −0.637 1.00 47.42 379 OG1 THR A 386 32.775 63.024 −1.744 1.00 50.45 380 CC2 THR A 386 34.615 64.347 −0.925 1.00 51.73 381 C THR A 386 35.487 62.132 0.681 1.00 46.45 382 O THR A 386 35.129 62.241 1.853 1.00 47.06 383 N ARG A 387 36.754 62.206 0.292 1.00 46.33 384 CA ARG A 387 37.849 62.410 1.228 1.00 46.50 385 CB ARG A 387 38.874 61.290 1.030 1.00 48.08 386 CC ARG A 387 40.086 61.366 1.933 1.00 54.89 387 CD AEG A 387 41.208 60.481 1.405 1.00 59.67 388 NE ARG A 387 42.438 60.668 2.165 1.00 63.12 389 CZ ARG A 387 42.775 59.950 3.230 1.00 65.65 390 NH1 ARG A 387 41.971 58.982 3.651 1.00 67.29 391 NH2 ARG A 387 43.899 60.215 3.889 1.00 63.40 392 C ARG A 387 38.517 63.786 1.046 1.00 46.30 393 O ARG A 387 38.733 64.239 −0.079 1.00 44.30 394 N LYS A 388 38.834 64.441 2.162 1.00 45.70 395 CA LYS A 388 39.489 65.749 2.140 1.00 44.68 396 CB LYS A 388 38.479 66.852 2.466 1.00 46.84 397 CG LYS A 388 37.337 66.931 1.476 1.00 56.94 398 CD LYS A 388 36.150 67.679 2.054 1.00 58.62 399 CE LYS A 388 34.883 67.307 1.309 1.00 61.92 400 NZ LYS A 388 33.676 67.856 1.977 1.00 70.07 401 C LYS A 388 40.646 65.798 3.143 1.00 44.52 402 O LYS A 388 40.502 65.379 4.294 1.00 40.60 403 N GLU A 389 41.793 66.304 2.689 1.00 47.26 404 CA GLU A 389 43.001 66.424 3.518 1.00 50.72 405 CB GLU A 389 44.114 65.531 2.965 1.00 54.88 406 CG GLU A 389 43.848 64.041 3.039 1.00 67.37 407 CD GLU A 389 44.979 63.225 2.436 1.00 75.83 408 OE1 GLU A 389 46.116 63.742 2.364 1.00 79.33 409 OE2 GLU A 389 44.738 62.062 2.044 1.00 80.70 410 C GLU A 389 43.510 67.871 3.551 1.00 51.11 411 O GLU A 389 43.644 68.510 2.504 1.00 48.28 412 N ALA A 390 43.814 68.382 4.741 1.00 52.07 413 CA ALA A 390 44.297 69.755 4.868 1.00 56.84 414 CB ALA A 390 43.120 70.712 4.972 1.00 53.86 415 C ALA A 390 45.229 69.957 6.058 1.00 60.96 416 O ALA A 390 45.085 69.315 7.098 1.00 61.14 417 N ALA A 391 46.179 70.873 5.896 1.00 65.61 418 CA ALA A 391 47.151 71.187 6.938 1.00 68.46 419 CB ALA A 391 48.398 70.336 6.761 1.00 71.73 420 C ALA A 391 47.518 72.661 6.866 1.00 70.37 421 O ALA A 391 47.076 73.461 7.688 1.00 72.17 422 N LEU A 397 47.315 68.210 11.080 1.00 60.70 423 CA LEU A 397 46.686 67.651 9.890 1.00 61.36 424 CD LEU A 397 47.489 66.458 9.375 1.00 64.28 425 CG LEU A 397 46.854 65.736 8.180 1.00 65.19 426 CD1 LEU A 397 46.802 66.670 6.981 1.00 65.40 427 CD2 LEU A 397 47.652 64.485 7.844 1.00 68.57 428 C LEU A 397 45.241 67.211 10.119 1.00 61.24 429 O LEU A 397 44.934 66.485 11.064 1.00 62.11 430 N THR A 398 44.360 67.654 9.233 1.00 59.83 431 CA THR A 398 42.950 67.309 9.305 1.00 58.04 432 CD THR A 398 42.061 68.572 9.263 1.00 58.72 433 OG1 THR A 398 42.171 69.278 10.506 1.00 64.28 434 CG2 THR A 398 40.608 68.197 9.023 1.00 61.55 435 C THR A 398 42.573 66.401 8.135 1.00 55.72 436 O THR A 398 43.021 66.595 7.000 1.00 55.02 437 N VAL A 399 41.752 65.401 8.422 1.00 52.38 438 CA VAL A 399 41.297 64.473 7.402 1.00 49.13 439 CB VAL A 399 42.143 63.179 7.391 1.00 51.57 440 CG1 VAL A 399 41.594 62.212 6.363 1.00 52.00 441 CG2 VAL A 399 43.590 63.500 7.068 1.00 55.81 442 C VAL A 399 39.847 64.093 7.643 1.00 46.27 443 O VAL A 399 39.478 63.649 8.732 1.00 43.17 444 N THR A 400 39.015 64.289 6.630 1.00 44.56 445 CA THR A 400 37.619 63.915 6.758 1.00 43.39 446 CB THR A 400 36.669 65.140 6.829 1.00 41.43 447 OG1 THR A 400 36.628 65.794 5.557 1.00 48.65 448 CG2 THR A 400 37.126 66.120 7.889 1.00 38.93 449 C THR A 400 37.174 63.059 5.584 1.00 40.85 450 O THR A 400 37.751 63.094 4.494 1.00 35.85 451 N SER A 401 36.146 62.267 5.847 1.00 39.13 452 CA SER A 401 35.542 61.417 4.847 1.00 37.93 453 CB SER A 401 35.885 59.944 5.079 1.00 40.15 454 OG SER A 401 35.290 59.142 4.069 1.00 44.51 455 C SER A 401 34.054 61.622 5.044 1.00 36.16 456 O SER A 401 33.552 61.461 6.153 1.00 36.19 457 N THR A 402 33.362 61.989 3.975 1.00 32.94 458 CA THR A 402 31.931 62.204 4.039 1.00 32.35 459 CB THR A 402 31.578 63.578 3.483 1.00 33.13 460 OG1 THR A 402 32.279 64.559 4.246 1.00 34.46 461 CG2 THR A 402 30.086 63.845 3.577 1.00 33.71 462 C THR A 402 31.222 61.117 3.243 1.00 31.66 463 O THR A 402 31.512 60.886 2.064 1.00 26.99 464 N LEU A 403 30.282 60.459 3.913 1.00 32.16 465 CA LEU A 403 29.526 59.370 3.319 1.00 32.46 466 CB LEU A 403 29.648 58.123 4.205 1.00 34.12 467 CG LEU A 403 28.920 56.838 3.794 1.00 34.78 468 CD1 LEU A 403 29.678 56.196 2.644 1.00 35.87 469 CD2 LEU A 403 28.856 55.873 4.968 1.00 31.42 470 C LEU A 403 28.052 59.690 3.099 1.00 33.39 471 O LEU A 403 27.321 60.005 4.040 1.00 30.14 472 N PRO A 404 27.604 59.633 1.835 1.00 34.13 473 CD PRO A 404 28.391 59.413 0.605 1.00 34.29 474 CA PRO A 404 26.203 59.899 1.513 1.00 34.91 475 CB PRO A 404 26.161 59.777 −0.008 1.00 33.92 476 CG PRO A 404 27.554 60.121 −0.426 1.00 33.77 477 C PRO A 404 25.427 58.773 2.191 1.00 36.43 478 O PRO A 404 25.824 57.610 2.140 1.00 30.87 479 N VAL A 405 24.326 59.120 2.835 1.00 37.52 480 CA VAL A 405 23.532 58.129 3.531 1.00 41.37 481 CB VAL A 405 23.522 58.462 5.053 1.00 44.39 482 CG1 VAL A 405 22.100 58.566 5.587 1.00 47.81 483 CG2 VAL A 405 24.312 57.420 5.799 1.00 43.63 484 C VAL A 405 22.108 58.056 2.980 1.00 42.93 485 O VAL A 405 21.558 59.047 2.511 1.00 42.10 486 N GLY A 406 21.518 56.868 3.019 1.00 45.32 487 CA GLY A 406 20.154 56.731 2.547 1.00 46.40 488 C GLY A 406 19.227 57.392 3.552 1.00 46.70 489 O GLY A 406 19.421 57.255 4.766 1.00 41.89 490 N THR A 407 18.227 58.114 3.048 1.00 46.37 491 CA THR A 407 17.259 58.809 3.892 1.00 49.05 492 CB THR A 407 16.252 59.617 3.038 1.00 51.01 493 OG1 THR A 407 16.929 60.700 2.391 1.00 55.76 494 CG2 THR A 407 15.147 60.177 3.905 1.00 54.66 495 C THR A 407 16.468 57.854 4.775 1.00 49.24 496 O THR A 407 16.446 58.003 5.995 1.00 48.91 497 N ALA A 408 15.823 56.874 4.147 1.00 49.71 498 CA ALA A 408 15.008 55.907 4.860 1.00 50.13 499 CB ALA A 408 14.233 55.038 3.876 1.00 53.74 500 C ALA A 408 15.823 55.031 5.788 1.00 51.25 501 O ALA A 408 15.393 54.748 6.909 1.00 50.28 502 N ASP A 409 16.995 54.600 5.330 1.00 50.74 503 CA ASP A 409 17.852 53.748 6.152 1.00 52.13 504 CB ASP A 409 19.102 53.335 5.370 1.00 58.27 505 CG ASP A 409 18.770 52.535 4.123 1.00 69.38 506 OD1 ASP A 409 18.105 51.479 4.252 1.00 75.94 507 OD2 ASP A 409 19.169 52.959 3.016 1.00 72.00 508 C ASP A 409 18.259 54.449 7.445 1.00 49.96 509 O ASP A 409 18.317 53.831 8.512 1.00 49.48 510 N TRP A 410 18.542 55.742 7.345 1.00 46.74 511 CA TRP A 410 18.931 56.494 8.517 1.00 44.75 512 CB TRP A 410 19.487 57.868 8.143 1.00 39.75 513 CG TRP A 410 19.913 58.601 9.362 1.00 37.35 514 CD2 TRP A 410 21.131 58.409 10.083 1.00 31.03 515 CE2 TRP A 410 21.049 59.188 11.254 1.00 29.68 516 CE3 TRP A 410 22.286 57.637 9.857 1.00 32.46 517 CD1 TRP A 410 19.166 59.481 10.099 1.00 32.61 518 NE1 TRP A 410 19.842 59.833 11.232 1.00 33.45 519 CZ2 TRP A 410 22.078 59.230 12.200 1.00 29.11 520 CZ3 TRP A 410 23.310 57.680 10.798 1.00 34.12 521 CH2 TRP A 410 23.195 58.472 11.958 1.00 35.80 522 C TRP A 410 17.743 56.666 9.451 1.00 43.08 523 O TRP A 410 17.867 56.463 10.655 1.00 38.95 524 N ILE A 411 16.593 57.037 8.894 1.00 46.39 525 CA ILE A 411 15.389 57.228 9.696 1.00 51.22 526 CB ILE A 411 14.218 57.752 8.841 1.00 53.02 527 CG2 ILE A 411 12.972 57.895 9.699 1.00 55.27 528 CG1 ILE A 411 14.590 59.112 8.240 1.00 56.63 529 CD1 ILE A 411 13.498 59.742 7.367 1.00 61.16 530 C ILE A 411 14.968 55.931 10.371 1.00 52.33 531 O ILE A 411 14.404 55.955 11.462 1.00 53.32 532 N GLU A 412 15.267 54.800 9.731 1.00 54.18 533 CA GLU A 412 14.907 53.501 10.279 1.00 53.56 534 CB GLU A 412 14.692 52.490 9.158 1.00 58.95 535 CG GUI A 412 13.298 52.566 8.572 1.00 73.61 536 CD GLU A 412 13.058 51.538 7.488 1.00 83.01 537 OE1 GLU A 412 13.415 50.356 7.689 1.00 89.18 538 OE2 GLU A 412 12.498 51.909 6.435 1.00 89.24 539 C GLU A 412 15.874 52.935 11.307 1.00 51.42 540 O GLU A 412 15.615 51.875 11.873 1.00 50.68 541 N GLY A 413 16.983 53.633 11.549 1.00 48.27 542 CA GLY A 413 17.929 53.172 12.549 1.00 46.15 543 C GLY A 413 19.223 52.489 12.133 1.00 44.58 544 O GLY A 413 19.925 51.963 12.994 1.00 42.91 545 N GLU A 414 19.556 52.482 10.844 1.00 44.06 546 CA GLU A 414 20.801 51.851 10.415 1.00 42.21 547 CB GLU A 414 21.077 52.133 8.928 1.00 42.27 548 CG GLU A 414 22.441 51.637 8.402 1.00 44.30 549 CD GLU A 414 22.564 50.113 8.361 1.00 52.18 550 OE1 GLU A 414 23.038 49.517 9.355 1.00 51.39 551 OE2 GLU A 414 22.175 49.510 7.336 1.00 49.53 552 C GLU A 414 21.910 52.453 11.261 1.00 41.40 553 O GLU A 414 21.819 53.605 11.687 1.00 38.41 554 N THR A 415 22.944 51.664 11.527 1.00 41.90 555 CA THR A 415 24.078 52.146 12.294 1.00 43.26 556 CB THR A 415 24.259 51.319 13.594 1.00 46.09 557 OG1 THR A 415 25.604 51.445 14.068 1.00 50.78 558 CG2 THR A 415 23.910 49.884 13.366 1.00 56.55 559 C THR A 415 25.330 52.101 11.410 1.00 41.87 560 O THR A 415 25.637 51.067 10.815 1.00 43.61 561 N TYR A 416 26.029 53.229 11.294 1.00 39.27 562 CA TYR A 416 27.222 53.291 10.450 1.00 37.37 563 CB TYR A 416 27.172 54.498 9.519 1.00 33.61 564 CG TYR A 416 25.967 54.536 8.622 1.00 27.57 565 CD1 TYR A 416 24.706 54.847 9.126 1.00 26.31 566 CE1 TYR A 416 23.591 54.848 8.300 1.00 35.08 567 CD2 TYR A 416 26.084 54.229 7.275 1.00 28.68 568 CE2 TYR A 416 24.985 54.221 6.449 1.00 30.56 569 CZ TYR A 416 23.743 54.530 6.960 1.00 35.62 570 OH TYR A 416 22.656 54.512 6.116 1.00 44.94 571 C TYR A 416 28.494 53.344 11.267 1.00 38.31 572 O TYR A 416 28.508 53.856 12.391 1.00 37.29 573 N GLN A 417 29.569 52.819 10.684 1.00 39.74 574 CA GLN A 417 30.849 52.777 11.364 1.00 40.75 575 CB GLN A 417 31.143 51.346 11.836 1.00 41.60 576 CG GLN A 417 32.360 51.247 12.751 1.00 53.57 577 CD GLN A 417 32.603 49.838 13.271 1.00 65.04 578 OE1 GLN A 417 33.476 49.119 12.775 1.00 69.74 579 NE2 GLN A 417 31.823 49.435 14.269 1.00 66.91 580 C GLN A 417 32.022 53.280 10.535 1.00 39.48 581 O GLN A 417 32.149 52.981 9.346 1.00 40.03 582 N CYS A 418 32.882 54.043 11.188 1.00 39.47 583 CA CYS A 418 34.075 54.568 10.559 1.00 41.39 584 C CYS A 418 35.246 53.868 11.232 1.00 41.00 585 O CYS A 418 35.395 53.939 12.452 1.00 41.94 586 CB CYS A 418 34.187 56.087 10.781 1.00 39.12 587 SG CYS A 418 35.688 56.818 10.050 1.00 53.87 588 N ALA A 419 36.059 53.171 10.446 1.00 42.75 589 CA ALA A 419 37.238 52.498 10.982 1.00 45.21 590 CB ALA A 419 37.357 51.073 10.412 1.00 45.00 591 C ALA A 419 38.462 53.335 10.602 1.00 46.28 592 O ALA A 419 38.826 53.428 9.429 1.00 44.60 593 N VAL A 420 39.088 53.961 11.592 1.00 49.65 594 CA VAL A 420 40.252 54.789 11.322 1.00 54.91 595 CB VAL A 420 40.295 56.016 12.245 1.00 52.57 596 CG1 VAL A 420 41.515 56.858 11.911 1.00 54.41 597 CG2 VAL A 420 39.032 56.844 12.083 1.00 52.89 598 C VAL A 420 41.564 54.028 11.477 1.00 59.75 599 O VAL A 420 41.877 53.517 12.556 1.00 56.32 600 N THR A 421 42.325 53.960 10.387 1.00 65.72 601 CA THR A 421 43.615 53.278 10.383 1.00 72.95 602 CB THR A 421 43.733 52.297 9.197 1.00 73.73 603 OG1 THR A 421 42.702 51.306 9.282 1.00 78.26 604 CG2 THR A 421 45.082 51.605 9.217 1.00 74.84 605 C THR A 421 44.741 54.298 10.269 1.00 76.77 606 O THR A 421 45.141 54.663 9.164 1.00 76.76 607 N ALA A 422 45.248 54.757 11.410 1.00 81.68 608 CA ALA A 422 46.330 55.738 11.427 1.00 86.81 609 CB ALA A 422 46.358 56.466 12.768 1.00 86.67 610 C ALA A 422 47.670 55.060 11.178 1.00 90.55 611 O ALA A 422 47.843 53.876 11.477 1.00 91.00 612 N PRO A 423 48.641 55.807 10.625 1.00 93.77 613 CD PRO A 423 48.615 57.260 10.385 1.00 94.85 614 CA PRO A 423 49.970 55.257 10.341 1.00 95.83 615 CB PRO A 423 50.731 56.459 9.791 1.00 96.70 616 CG PRO A 423 50.074 57.619 10.487 1.00 97.10 617 C PRO A 423 50.612 54.674 11.596 1.00 97.16 618 O PRO A 423 50.850 53.472 11.674 1.00 97.34 619 N ALA A 424 50.893 55.524 12.578 1.00 98.50 620 CA ALA A 424 51.486 55.063 13.829 1.00 99.73 621 CB ALA A 424 51.995 56.252 14.626 1.00 99.11 622 C ALA A 424 50.412 54.318 14.625 1.00 100.69 623 O ALA A 424 49.503 53.725 14.046 1.00 101.64 624 N LEU A 425 50.521 54.355 15.950 1.00 100.65 625 CA LEU A 425 49.550 53.705 16.828 1.00 99.91 626 CB LEU A 425 48.182 54.372 16.671 1.00 100.27 627 CG LEU A 425 48.126 55.833 17.125 1.00 102.88 628 CD1 LEU A 425 46.735 56.386 16.889 1.00 102.68 629 CD2 LEU A 425 48.498 55.932 18.603 1.00 105.00 630 C LEU A 425 49.427 52.200 16.586 1.00 98.82 631 O LEU A 425 49.985 51.676 15.629 1.00 98.87 632 N PRO A 426 48.712 51.485 17.475 1.00 97.69 633 CD PRO A 426 48.418 51.939 18.849 1.00 98.02 634 CA PRO A 426 48.513 50.034 17.361 1.00 95.83 635 CB PRO A 426 48.673 49.570 18.797 1.00 96.48 636 CG PRO A 426 47.965 50.659 19.545 1.00 96.97 637 C PRO A 426 47.145 49.651 16.791 1.00 94.21 638 O PRO A 426 47.006 49.360 15.602 1.00 94.03 639 N ARG A 427 46.140 49.637 17.661 1.00 92.33 640 CA ARG A 427 44.778 49.297 17.269 1.00 90.72 641 CB ARG A 427 43.928 49.017 18.510 1.00 92.36 642 CG ARG A 427 44.349 47.816 19.342 1.00 96.36 643 CD ARG A 427 43.525 46.585 18.998 1.00 99.46 644 NE ARG A 427 43.247 45.778 20.184 1.00 101.30 645 CZ ARG A 427 42.540 46.203 21.228 1.00 102.28 646 NE1 ARG A 427 42.037 47.430 21.236 1.00 102.89 647 NH2 ARG A 427 42.334 45.400 22.264 1.00 102.96 648 C ARG A 427 44.152 50.458 16.505 1.00 88.67 649 O ARG A 427 44.292 51.614 16.902 1.00 88.90 650 N ALA A 428 43.462 50.153 15.413 1.00 85.79 651 CA ALA A 428 42.807 51.188 14.631 1.00 82.45 652 CB ALA A 428 42.310 50.615 13.311 1.00 82.49 653 C ALA A 428 41.637 51.707 15.456 1.00 79.74 654 O ALA A 428 41.032 50.955 16.221 1.00 79.87 655 N LEU A 429 41.330 52.994 15.315 1.00 76.91 656 CA LEU A 429 40.223 53.604 16.049 1.00 72.60 657 CB LEU A 429 40.405 55.125 16.126 1.00 73.30 658 CG LEU A 429 41.684 55.685 16.757 1.00 75.14 659 CD1 LEU A 429 41.706 57.197 16.600 1.00 70.88 660 CD2 LEU A 429 41.756 55.296 18.227 1.00 79.00 661 C LEU A 429 38.921 53.290 15.323 1.00 69.58 662 O LEU A 429 38.894 53.209 14.094 1.00 67.68 663 N MET A 430 37.845 53.116 16.085 1.00 66.58 664 CA MET A 430 36.543 52.815 15.504 1.00 63.72 665 CB MET A 430 36.203 51.340 15.704 1.00 66.69 666 CG MET A 430 37.237 50.395 15.125 1.00 76.81 667 SD MET A 430 36.764 48.668 15.345 1.00 89.36 668 CE MET A 430 36.990 48.471 17.110 1.00 87.45 669 C MET A 430 35.450 53.674 16.119 1.00 59.15 670 O MET A 430 35.371 53.822 17.340 1.00 59.09 671 N ARG A 431 34.607 54.245 15.267 1.00 55.24 672 CA ARG A 431 33.523 55.091 15.746 1.00 51.07 673 CB ARG A 431 33.863 56.564 15.516 1.00 51.17 674 CG ARG A 431 35.291 56.939 15.897 1.00 55.59 675 CD ARG A 431 35.320 58.159 16.805 1.00 67.55 676 NE ARG A 431 35.147 57.816 18.216 1.00 74.62 677 CZ ARG A 431 36.128 57.380 19.001 1.00 76.90 678 NH1 ARG A 431 37.353 57.236 18.514 1.00 77.02 679 NH2 ARG A 431 35.888 57.087 20.274 1.00 79.64 680 C ARG A 431 32.244 54.732 15.013 1.00 47.90 681 O ARG A 431 32.277 54.386 13.832 1.00 46.26 682 N SER A 432 31.120 54.812 15.715 1.00 45.54 683 CA SER A 432 29.832 54.495 15.112 1.00 45.94 684 CB SER A 432 29.356 53.116 15.584 1.00 47.12 685 OG SER A 432 29.331 53.040 16.994 1.00 50.92 686 C SER A 432 28.764 55.537 15.412 1.00 43.27 687 O SER A 432 28.862 56.272 16.391 1.00 42.70 688 N THR A 433 27.736 55.588 14.569 1.00 40.97 689 CA THR A 433 26.663 56.552 14.758 1.00 38.90 690 CB THR A 433 26.967 57.875 14.027 1.00 39.50 691 OG1 THR A 433 25.911 58.808 14.280 1.00 38.91 692 CG2 THR A 433 27.093 57.646 12.516 1.00 36.51 693 C THR A 433 25.329 56.017 14.262 1.00 39.62 694 O THR A 433 25.283 55.188 13.356 1.00 39.87 695 N THR A 434 24.249 56.495 14.876 1.00 39.10 696 CA THR A 434 22.889 56.101 14.531 1.00 39.67 697 CB THR A 434 22.480 54.812 15.282 1.00 43.40 698 OG1 THR A 434 22.307 55.104 16.675 1.00 53.59 699 CG2 THR A 434 23.559 53.770 15.171 1.00 52.29 700 C THR A 434 21.939 57.220 14.969 1.00 38.41 701 O THR A 434 22.325 58.110 15.726 1.00 38.84 702 N ALA A 435 20.701 57.179 14.506 1.00 37.73 703 CA ALA A 435 19.747 58.190 14.911 1.00 44.38 704 CB ALA A 435 18.426 57.968 14.213 1.00 40.72 705 C ALA A 435 19.577 58.033 16.421 1.00 47.78 706 O ALA A 435 19.611 56.919 16.937 1.00 46.98 707 N THR A 436 19.413 59.146 17.129 1.00 52.31 708 CA THR A 436 19.217 59.094 18.574 1.00 55.83 709 CB THR A 436 19.492 60.469 19.240 1.00 59.83 710 OG1 THR A 436 20.873 60.816 19.072 1.00 62.64 711 CG2 THR A 436 19.159 60.425 20.732 1.00 60.56 712 C THR A 436 17.766 58.707 18.840 1.00 56.91 713 O THR A 436 16.852 59.242 18.212 1.00 55.51 714 N SER A 437 17.557 57.759 19.748 1.00 58.87 715 CA SER A 437 16.202 57.344 20.095 1.00 61.80 716 CB SER A 437 16.155 55.854 20.474 1.00 63.69 717 OG SER A 437 16.984 55.571 21.589 1.00 67.24 718 C SER A 437 15.753 58.203 21.272 1.00 61.35 719 O SER A 437 16.477 59.111 21.690 1.00 61.92 720 N GLY A 438 14.567 57.930 21.803 1.00 60.43 721 CA GLY A 438 14.087 58.719 22.923 1.00 59.27 722 C GLY A 438 12.999 59.691 22.510 1.00 58.25 723 O GLY A 438 12.739 59.847 21.321 1.00 58.13 724 N PRO A 439 12.347 60.363 23.472 1.00 58.84 725 CD PRO A 439 12.555 60.215 24.923 1.00 60.09 726 CA PRO A 439 11.275 61.323 23.203 1.00 57.04 727 CB PRO A 439 10.908 61.832 24.597 1.00 57.59 728 CG PRO A 439 11.224 60.667 25.472 1.00 59.40 729 C PRO A 439 11.691 62.453 22.272 1.00 54.66 730 O PRO A 439 12.877 62.776 22.155 1.00 56.08 731 N ARG A 440 10.703 63.052 21.618 1.00 51.95 732 CA ARG A 440 10.942 64.149 20.695 1.00 49.50 733 CB ARG A 440 10.471 63.771 19.283 1.00 51.89 734 CG ARG A 440 10.921 62.400 18.791 1.00 59.84 735 CD ARG A 440 12.412 62.334 18.465 1.00 66.22 736 NE ARG A 440 12.845 60.943 18.313 1.00 74.61 737 CZ ARG A 440 14.047 60.555 17.896 1.00 76.10 738 NH1 ARG A 440 14.967 61.444 17.573 1.00 77.20 739 NH2 ARG A 440 14.328 59.262 17.805 1.00 84.96 740 C ARG A 440 10.145 65.351 21.190 1.00 46.80 741 O ARG A 440 9.058 65.194 21.746 1.00 46.09 742 N ALA A 441 10.696 66.547 21.001 1.00 42.67 743 CA ALA A 441 10.024 67.779 21.402 1.00 39.13 744 CB ALA A 441 10.384 68.142 22.837 1.00 32.25 745 C ALA A 441 10.452 68.888 20.454 1.00 39.00 746 O ALA A 441 11.639 69.045 20.175 1.00 38.16 747 N ALA A 442 9.482 69.651 19.964 1.00 37.20 748 CA ALA A 442 9.736 70.739 19.037 1.00 37.26 749 CB ALA A 442 8.413 71.288 18.526 1.00 37.47 750 C ALA A 442 10.568 71.882 19.617 1.00 39.85 751 O ALA A 442 10.612 72.090 20.825 1.00 41.57 752 N PRO A 443 11.246 72.640 18.743 1.00 39.83 753 CD PRO A 443 11.478 72.297 17.334 1.00 40.96 754 CA PRO A 443 12.080 73.775 19.131 1.00 38.29 755 CB PRO A 443 13.058 73.922 17.956 1.00 36.98 756 CG PRO A 443 12.907 72.675 17.168 1.00 36.14 757 C PRO A 443 11.220 75.037 19.272 1.00 40.19 758 O PRO A 443 10.204 75.194 18.588 1.00 40.51 759 N ALA A 444 11.636 75.927 20.163 1.00 39.07 760 CA ALA A 444 10.942 77.188 20.376 1.00 36.58 761 CD ALA A 444 10.605 77.372 21.860 1.00 40.22 762 C ALA A 444 11.962 78.227 19.919 1.00 34.33 763 O ALA A 444 13.109 78.242 20.398 1.00 30.65 764 N VAL A 445 11.543 79.081 18.991 1.00 28.37 765 CA VAL A 445 12.428 80.080 18.436 1.00 26.39 766 GB VAL A 445 12.448 79.948 16.902 1.00 26.69 767 CG1 VAL A 445 13.395 80.980 16.310 1.00 23.97 768 CG2 VAL A 445 12.853 78.524 16.514 1.00 22.56 769 C VAL A 445 12.103 81.532 18.809 1.00 27.26 770 O VAL A 445 10.956 81.954 18.733 1.00 24.12 771 N TYR A 446 13.127 82.281 19.207 1.00 23.45 772 CA TYR A 446 12.955 83.681 19.559 1.00 25.54 773 CB TYR A 446 12.868 83.878 21.085 1.00 24.97 774 CC TYR A 446 12.704 85.336 21.440 1.00 24.95 775 CD1 TYR A 446 11.639 86.083 20.918 1.00 37.39 776 CE1 TYR A 446 11.506 87.454 21.193 1.00 34.09 777 CD2 TYR A 446 13.627 85.987 22.249 1.00 28.20 778 CE2 TYR A 446 13.508 87.355 22.533 1.00 31.02 779 CZ TYR A 446 12.440 88.081 21.998 1.00 34.30 780 OH TYR A 446 12.306 89.426 22.254 1.00 35.42 781 C TYR A 446 14.135 84.470 19.012 1.00 23.87 782 O TYR A 446 15.275 84.279 19.437 1.00 28.38 783 N ALA A 447 13.858 85.346 18.058 1.00 26.40 784 CA ALA A 447 14.893 86.155 17.429 1.00 27.30 785 CB ALA A 447 14.766 86.065 15.905 1.00 24.55 786 C ALA A 447 14.760 87.598 17.898 1.00 30.87 787 O ALA A 447 13.655 88.085 18.121 1.00 32.42 788 N PHE A 448 15.880 88.290 18.055 1.00 31.33 789 CA PHE A 448 15.801 89.661 18.518 1.00 34.25 790 CB PHE A 448 15.616 89.662 20.040 1.00 40.48 791 CG PHE A 448 16.795 89.103 20.786 1.00 39.26 792 CD1 PHE A 448 17.837 89.937 21.177 1.00 39.27 793 CD2 PHE A 448 16.896 87.738 21.041 1.00 36.97 794 CE1 PHE A 448 18.967 89.420 21.814 1.00 43.41 795 CE2 PHE A 448 18.022 87.211 21.678 1.00 36.78 796 CZ PHE A 448 19.059 88.054 22.064 1.00 37.14 797 C PHE A 448 17.021 90.487 18.148 1.00 34.75 798 O PHE A 448 18.046 89.954 17.731 1.00 34.97 799 N ALA A 449 16.892 91.799 18.302 1.00 37.02 800 CA ALA A 449 17.977 92.723 18.021 1.00 38.65 801 CB ALA A 449 17.478 93.869 17.202 1.00 32.34 802 C ALA A 449 18.550 93.250 19.333 1.00 42.92 803 O ALA A 449 17.826 93.435 20.306 1.00 42.07 804 N THR A 450 19.857 93.489 19.341 1.00 47.71 805 CA THR A 450 20.552 94.014 20.503 1.00 52.16 806 CB THR A 450 22.023 93.560 20.501 1.00 53.90 807 OG1 THR A 450 22.078 92.132 20.415 1.00 61.82 808 CG2 THR A 450 22.723 94.006 21.773 1.00 62.58 809 C THR A 450 20.503 95.547 20.493 1.00 54.69 810 O THR A 450 20.617 96.179 19.441 1.00 51.28 811 N PRO A 451 20.320 96.161 21.669 1.00 57.24 812 CD PRO A 451 19.982 95.539 22.963 1.00 60.66 813 CA PRO A 451 20.261 97.623 21.762 1.00 61.04 814 CB PRO A 451 20.029 97.864 23.254 1.00 61.38 815 CG PRO A 451 19.240 96.654 23.667 1.00 63.63 816 C PRO A 451 21.537 98.299 21.253 1.00 63.11 817 O PRO A 451 22.651 97.918 21.616 1.00 61.66 818 N GLU A 452 21.370 99.297 20.394 1.00 66.04 819 CA GLU A 452 22.517 100.025 19.863 1.00 69.40 820 CB GLU A 452 22.646 99.800 18.347 1.00 67.34 821 CG GLU A 452 24.095 99.689 17.823 1.00 60.86 822 CD GLU A 452 24.785 98.375 18.224 1.00 59.08 823 OE1 GLU A 452 24.090 97.345 18.325 1.00 62.62 824 OE2 GLU A 452 26.022 98.351 18.424 1.00 45.82 825 C GLU A 452 22.322 101.510 20.170 1.00 71.98 826 O GLU A 452 21.705 102.240 19.395 1.00 70.35 827 N ALA A 453 22.842 101.941 21.317 1.00 75.33 828 CA ALA A 453 22.733 103.334 21.753 1.00 78.80 829 CB ALA A 453 23.482 103.525 23.071 1.00 80.74 830 C ALA A 453 23.260 104.318 20.706 1.00 80.53 831 O ALA A 453 24.167 104.001 19.933 1.00 82.95 832 N LYS A 459 29.802 96.915 16.453 1.00 51.87 833 CA LYS A 459 28.953 96.350 15.407 1.00 52.84 834 CB LYS A 459 29.613 95.121 14.783 1.00 55.20 835 CG LYS A 459 30.879 95.429 14.011 1.00 63.98 836 CD LYS A 459 31.199 94.329 13.012 1.00 72.67 837 CE LYS A 459 30.116 94.234 11.943 1.00 77.63 838 NZ LYS A 459 30.478 93.298 10.841 1.00 83.78 839 C LYS A 459 27.567 95.962 15.905 1.00 50.86 840 O LYS A 459 27.426 95.389 16.982 1.00 49.65 841 N ARG A 460 26.555 96.268 15.099 1.00 48.30 842 CA ARG A 460 25.167 95.960 15.426 1.00 47.61 843 CB ARG A 460 24.250 96.735 14.480 1.00 51.65 844 CG ARG A 460 24.571 98.229 14.509 1.00 59.85 845 CD ARG A 460 23.816 99.030 13.465 1.00 65.41 846 NE ARG A 460 24.200 100.442 13.497 1.00 70.36 847 CZ ARG A 460 25.426 100.898 13.252 1.00 73.06 848 NH1 ARG A 460 26.412 100.060 12.950 1.00 75.61 849 NH2 ARG A 460 25.671 102.199 13.309 1.00 76.52 850 C ARG A 460 24.936 94.446 15.341 1.00 44.39 851 O ARG A 460 25.542 93.761 14.511 1.00 41.11 852 N THR A 461 24.060 93.928 16.195 1.00 40.18 853 CA THR A 461 23.832 92.489 16.250 1.00 40.02 854 CB THR A 461 24.615 91.867 17.441 1.00 41.84 855 OG1 THR A 461 25.999 92.217 17.350 1.00 52.98 856 CG2 THR A 461 24.498 90.362 17.434 1.00 48.91 857 C THR A 461 22.393 92.026 16.401 1.00 37.19 858 O THR A 461 21.591 92.641 17.118 1.00 37.94 859 N LEU A 462 22.088 90.919 15.725 1.00 33.00 860 CA LEU A 462 20.791 90.265 15.811 1.00 29.46 861 CB LEU A 462 20.166 90.050 14.433 1.00 30.35 862 CG LEU A 462 19.922 91.318 13.602 1.00 33.09 863 CD1 LEU A 462 19.188 90.961 12.315 1.00 32.32 864 CD2 LEU A 462 19.101 92.307 14.401 1.00 25.52 865 C LEU A 462 21.161 88.928 16.438 1.00 29.44 866 O LEU A 462 22.261 88.416 16.206 1.00 24.62 867 N ALA A 463 20.257 88.363 17.232 1.00 27.23 868 CA ALA A 463 20.550 87.114 17.908 1.00 27.78 869 CB ALA A 463 21.112 87.401 19.310 1.00 26.61 870 C ALA A 463 19.299 86.268 17.996 1.00 28.37 871 O ALA A 463 18.185 86.776 17.867 1.00 29.09 872 N CYS A 464 19.485 84.977 18.230 1.00 22.40 873 CA CYS A 464 18.354 84.066 18.279 1.00 26.72 874 C CYS A 464 18.562 82.978 19.314 1.00 24.16 875 O CYS A 464 19.648 82.401 19.409 1.00 23.01 876 CB CYS A 464 18.190 83.428 16.900 1.00 24.58 877 SG CYS A 464 16.806 82.273 16.677 1.00 40.31 878 N LEU A 465 17.504 82.692 20.068 1.00 22.68 879 CA LEU A 465 17.548 81.650 21.087 1.00 24.31 880 CB LEU A 465 17.127 82.210 22.460 1.00 26.81 881 CG LEU A 465 16.759 81.181 23.546 1.00 21.10 882 CD1 LEU A 465 17.941 80.290 23.849 1.00 21.73 883 CD2 LEU A 465 16.338 81.900 24.807 1.00 30.90 884 C LEU A 465 16.587 80.557 20.647 1.00 23.79 885 O LEU A 465 15.417 80.830 20.359 1.00 22.87 886 N ILE A 466 17.079 79.324 20.590 1.00 23.16 887 CA ILE A 466 16.251 78.198 20.174 1.00 23.50 888 CB ILE A 466 16.762 77.582 18.849 1.00 23.66 889 CG2 ILE A 466 15.800 76.460 18.395 1.00 29.47 890 CG1 ILE A 466 16.861 78.687 17.780 1.00 19.89 891 CD1 ILE A 466 17.371 78.202 16.450 1.00 36.91 892 C ILE A 466 16.326 77.212 21.316 1.00 22.24 893 O ILE A 466 17.411 76.789 21.715 1.00 24.74 894 N GLN A 467 15.167 76.811 21.830 1.00 23.91 895 CA GLN A 467 15.182 75.958 23.005 1.00 31.01 896 CB GLN A 467 15.224 76.853 24.254 1.00 30.11 897 CG GLN A 467 13.993 77.731 24.446 1.00 26.37 898 CD GLN A 467 14.114 78.680 25.636 1.00 29.83 899 OE1 GLN A 467 14.890 78.464 26.579 1.00 28.59 900 NE2 GLN A 467 13.318 79.731 25.605 1.00 31.49 901 C GLN A 467 14.054 74.959 23.148 1.00 33.72 902 O GLN A 467 13.131 74.909 22.332 1.00 31.53 903 N ASN A 468 14.179 74.158 24.205 1.00 38.27 904 CA ASN A 468 13.215 73.135 24.574 1.00 41.08 905 CB ASN A 468 11.856 73.761 24.855 1.00 43.70 906 CG ASN A 468 11.949 74.935 25.797 1.00 50.48 907 OD1 ASN A 468 12.641 74.878 26.819 1.00 59.45 908 ND2 ASN A 468 11.243 76.006 25.472 1.00 56.28 909 C ASN A 468 13.052 72.040 23.546 1.00 41.04 910 O ASN A 468 11.986 71.445 23.440 1.00 38.53 911 N PHE A 469 14.101 71.757 22.791 1.00 38.66 912 CA PHE A 469 13.996 70.706 21.797 1.00 38.07 913 CB PHE A 469 14.419 71.240 20.427 1.00 29.35 914 CG PHE A 469 15.888 71.536 20.309 1.00 28.48 915 CD1 PHE A 469 16.785 70.541 19.987 1.00 23.56 916 CD2 PHE A 469 16.369 72.823 20.521 1.00 24.16 917 CE1 PHE A 469 18.137 70.816 19.872 1.00 27.41 918 CE2 PHE A 469 17.733 73.107 20.409 1.00 32.69 919 CZ PHE A 469 18.616 72.094 20.083 1.00 24.40 920 C PHE A 469 14.815 69.475 22.161 1.00 38.11 921 O PHE A 469 15.848 69.574 22.813 1.00 39.11 922 N MET A 470 14.333 68.313 21.741 1.00 40.05 923 CA MET A 470 15.001 67.031 21.970 1.00 41.39 924 CB MET A 470 14.618 66.417 23.321 1.00 46.13 925 CG MET A 470 13.159 66.043 23.530 1.00 60.40 926 SD MET A 470 12.863 65.634 25.280 1.00 65.64 927 CE MET A 470 13.541 63.941 25.373 1.00 71.36 928 C MET A 470 14.505 66.183 20.820 1.00 38.04 929 O MET A 470 13.327 66.224 20.482 1.00 36.87 930 N PRO A 471 15.399 65.416 20.175 1.00 37.84 931 CD PRO A 471 14.946 64.687 18.983 1.00 38.40 932 CA PRO A 471 16.853 65.240 20.358 1.00 37.04 933 CB PRO A 471 17.200 64.115 19.368 1.00 38.82 934 CG PRO A 471 15.852 63.524 19.004 1.00 40.26 935 C PRO A 471 17.685 66.508 20.104 1.00 35.06 936 O PRO A 471 17.157 67.524 19.668 1.00 33.27 937 N GLU A 472 18.989 66.420 20.340 1.00 35.63 938 CA GLU A 472 19.895 67.567 20.202 1.00 38.83 939 CB GLU A 472 21.169 67.308 20.991 1.00 43.92 940 CG GLU A 472 22.084 66.301 20.308 1.00 54.98 941 CD GLU A 472 23.312 65.943 21.137 1.00 65.38 942 OE1 GLU A 472 23.431 66.428 22.279 1.00 73.96 943 OE2 GLU A 472 24.158 65.167 20.650 1.00 71.17 944 C GLU A 472 20.308 68.032 18.806 1.00 36.65 945 O GLU A 472 20.799 69.147 18.649 1.00 32.41 946 N ASP A 473 20.118 67.198 17.789 1.00 35.48 947 CA ASP A 473 20.508 67.596 16.432 1.00 34.00 948 CB ASP A 473 20.534 66.375 15.506 1.00 39.24 949 CG ASP A 473 21.607 65.361 15.907 1.00 48.86 950 OD1 ASP A 473 22.724 65.800 16.283 1.00 42.86 951 OD2 ASP A 473 21.330 64.139 15.835 1.00 46.87 952 C ASP A 473 19.607 68.683 15.844 1.00 34.33 953 O ASP A 473 18.380 68.543 15.785 1.00 34.18 954 N ILE A 474 20.216 69.776 15.409 1.00 27.93 955 CA ILE A 474 19.435 70.862 14.846 1.00 28.40 956 CB ILE A 474 18.874 71.752 15.971 1.00 25.16 957 CG2 ILE A 474 19.998 72.564 16.611 1.00 26.53 958 CG1 ILE A 474 17.772 72.665 15.436 1.00 21.56 959 CD1 ILE A 474 17.009 73.381 16.593 1.00 23.93 960 C ILE A 474 20.274 71.710 13.910 1.00 26.83 961 O ILE A 474 21.473 71.827 14.086 1.00 25.94 962 N SER A 475 19.625 72.275 12.898 1.00 24.54 963 CA SER A 475 20.264 73.154 11.933 1.00 23.71 964 CB SER A 475 20.014 72.668 10.510 1.00 22.00 965 OG SER A 475 20.555 71.379 10.341 1.00 30.00 966 C SER A 475 19.633 74.529 12.117 1.00 24.55 967 O SER A 475 18.410 74.669 12.135 1.00 23.24 968 N VAL A 476 20.476 75.542 12.253 1.00 24.48 969 CA VAL A 476 20.038 76.908 12.446 1.00 26.25 970 CB VAL A 476 20.672 77.503 13.721 1.00 24.14 971 CG1 VAL A 476 20.260 78.965 13.873 1.00 23.36 972 CG2 VAL A 476 20.243 76.693 14.937 1.00 28.16 973 C VAL A 476 20.489 77.723 11.253 1.00 28.80 974 O VAL A 476 21.607 77.555 10.761 1.00 32.13 975 N GLN A 477 19.629 78.607 10.774 1.00 28.79 976 CA GLN A 477 20.011 79.424 9.642 1.00 30.02 977 CB GLN A 477 19.746 78.687 8.326 1.00 31.30 978 CG GLN A 477 18.330 78.240 8.107 1.00 46.28 979 CD GLN A 477 18.232 77.101 7.093 1.00 49.95 980 OE1 GLN A 477 17.145 76.758 6.635 1.00 51.94 981 NE2 GLN A 477 19.373 76.503 6.751 1.00 51.51 982 C GLN A 477 19.287 80.744 9.669 1.00 30.41 983 O GLN A 477 18.185 80.843 10.198 1.00 30.03 984 N TRP A 478 19.941 81.759 9.124 1.00 29.86 985 CA TRP A 478 19.390 83.095 9.058 1.00 29.12 986 CB TRP A 478 20.435 84.101 9.521 1.00 31.11 987 CG TRP A 478 20.664 84.073 10.988 1.00 36.98 988 CD2 TRP A 478 19.995 84.874 11.968 1.00 34.77 989 CE2 TRP A 478 20.516 84.508 13.230 1.00 37.75 990 CE3 TRP A 478 18.998 85.858 11.906 1.00 31.61 991 CD1 TRP A 478 21.540 83.280 11.668 1.00 35.86 992 NE1 TRP A 478 21.458 83.535 13.014 1.00 35.58 993 CZ2 TRP A 478 20.079 85.106 14.432 1.00 26.96 994 CZ3 TRP A 478 18.561 86.452 13.095 1.00 35.86 995 CH2 TRP A 478 19.103 86.069 14.343 1.00 31.66 996 C TRP A 478 18.952 83.425 7.632 1.00 29.01 997 O TRP A 478 19.594 83.020 6.661 1.00 24.19 998 N LEU A 479 17.858 84.164 7.518 1.00 31.15 999 CA LEU A 479 17.325 84.558 6.220 1.00 36.67 1000 CB LEU A 479 16.063 83.763 5.902 1.00 41.07 1001 CG LEU A 479 16.016 82.272 6.233 1.00 48.71 1002 CD1 LEU A 479 14.739 81.711 5.660 1.00 57.57 1003 CD2 LEU A 479 17.204 81.546 5.645 1.00 56.00 1004 C LEU A 479 16.976 86.044 6.180 1.00 38.99 1005 O LEU A 479 16.602 86.635 7.191 1.00 37.96 1006 N HIS A 480 17.100 86.637 5.004 1.00 42.00 1007 CA HIS A 480 16.766 88.039 4.816 1.00 48.67 1008 CB HIS A 480 17.952 88.816 4.229 1.00 50.22 1009 CG HIS A 480 17.706 90.291 4.086 1.00 53.99 1010 CD2 HIS A 480 18.559 91.344 4.107 1.00 56.80 1011 ND1 HIS A 480 16.453 90.821 3.861 1.00 54.56 1012 CE1 HIS A 480 16.543 92.135 3.752 1.00 60.76 1013 NE2 HIS A 480 17.811 92.478 3.897 1.00 59.92 1014 C HIS A 480 15.628 87.975 3.817 1.00 52.66 1015 O HIS A 480 15.823 88.174 2.618 1.00 51.85 1016 N ASN A 481 14.439 87.655 4.320 1.00 58.88 1017 CA ASN A 481 13.261 87.538 3.472 1.00 63.74 1018 CB ASN A 481 13.012 88.837 2.693 1.00 69.70 1019 CG ASN A 481 12.389 89.926 3.539 1.00 76.04 1020 OD1 ASN A 481 12.354 91.087 3.138 1.00 80.67 1021 ND2 ASN A 481 11.881 89.558 4.708 1.00 82.88 1022 C ASN A 481 13.466 86.418 2.467 1.00 63.93 1023 O ASN A 481 14.198 86.592 1.496 1.00 67.09 1024 N GLU A 482 12.819 85.278 2.701 1.00 62.43 1025 CA GLU A 482 12.885 84.123 1.801 1.00 60.15 1026 CB GLU A 482 11.977 84.375 0.581 1.00 65.85 1027 CG GLU A 482 11.579 85.846 0.393 1.00 78.14 1028 CD GLU A 482 11.654 86.318 −1.044 1.00 84.88 1029 OE1 GLU A 482 12.616 85.938 −1.746 1.00 90.19 1030 OE2 GLU A 482 10.759 87.082 −1.466 1.00 87.19 1031 C GLU A 482 14.269 83.651 1.314 1.00 54.93 1032 O GLU A 482 14.406 82.516 0.853 1.00 57.04 1033 N VAL A 483 15.295 84.489 1.414 1.00 49.03 1034 CA VAL A 483 16.613 84.089 0.937 1.00 45.46 1035 CB VAL A 483 17.209 85.150 −0.026 1.00 43.71 1036 CG1 VAL A 483 17.320 86.501 0.673 1.00 50.19 1037 CG2 VAL A 483 18.567 84.687 −0.533 1.00 43.76 1038 C VAL A 483 17.584 83.842 2.078 1.00 43.31 1039 O VAL A 483 17.741 84.676 2.963 1.00 41.21 1040 N GLN A 484 18.238 82.687 2.039 1.00 42.10 1041 CA GLN A 484 19.189 82.297 3.064 1.00 41.31 1042 CB GLN A 484 19.349 80.778 3.053 1.00 46.93 1043 CG GLN A 484 20.420 80.262 3.993 1.00 54.66 1044 CD GLN A 484 20.428 78.749 4.101 1.00 61.50 1045 OE1 GLN A 484 21.402 78.158 4.568 1.00 65.59 1046 NE2 GLN A 484 19.333 78.114 3.684 1.00 62.36 1047 C GLN A 484 20.564 82.958 2.959 1.00 40.69 1048 O GLN A 484 21.124 83.097 1.868 1.00 39.56 1049 N LEU A 485 21.098 83.358 4.111 1.00 34.74 1050 CA LEU A 485 22.408 83.998 4.191 1.00 36.73 1051 CB LEU A 485 22.511 84.879 5.445 1.00 36.78 1052 CG LEU A 485 21.501 86.011 5.643 1.00 38.16 1053 CD1 LEU A 485 21.769 86.724 6.966 1.00 39.22 1054 CD2 LEU A 485 21.607 86.969 4.479 1.00 41.68 1055 C LEU A 485 23.485 82.923 4.266 1.00 36.82 1056 O LEU A 485 23.212 81.795 4.660 1.00 34.53 1057 N PRO A 486 24.725 83.258 3.883 1.00 40.02 1058 CD PRO A 486 25.251 84.563 3.448 1.00 39.74 1059 CA PRO A 486 25.791 82.249 3.949 1.00 45.08 1060 CB PRO A 486 27.018 82.994 3.422 1.00 44.97 1061 CG PRO A 486 26.457 84.162 2.661 1.00 41.94 1062 C PRO A 486 25.971 81.862 5.413 1.00 49.91 1063 O PRO A 486 25.830 82.711 6.291 1.00 49.23 1064 N ASP A 487 26.291 80.599 5.677 1.00 54.02 1065 CA ASP A 487 26.486 80.131 7.046 1.00 58.50 1066 CB ASP A 487 26.851 78.647 7.039 1.00 68.77 1067 CG ASP A 487 26.662 77.993 8.392 1.00 79.77 1068 OD1 ASP A 487 27.164 78.545 9.397 1.00 87.08 1069 OD2 ASP A 487 26.016 76.921 8.448 1.00 87.04 1070 C ASP A 487 27.594 80.928 7.746 1.00 57.99 1071 O ASP A 487 27.445 81.352 8.898 1.00 58.25 1072 N ALA A 488 28.695 81.135 7.029 1.00 55.74 1073 CA ALA A 488 29.852 81.861 7.546 1.00 55.27 1074 CB ALA A 488 30.833 82.122 6.418 1.00 55.02 1075 C ALA A 488 29.511 83.177 8.239 1.00 54.82 1076 O ALA A 488 30.326 83.726 8.983 1.00 55.09 1077 N ARG A 489 28.307 83.682 8.004 1.00 52.93 1078 CA ARG A 489 27.899 84.944 8.599 1.00 48.90 1079 CB ARG A 489 26.799 85.571 7.749 1.00 47.45 1080 CG ARG A 489 27.336 86.343 6.563 1.00 49.40 1081 CD ARG A 489 27.263 87.828 6.844 1.00 52.76 1082 NE ARG A 489 26.103 88.426 6.190 1.00 60.57 1083 CZ ARG A 489 25.513 89.559 6.560 1.00 60.40 1084 NH1 ARG A 489 25.959 90.247 7.604 1.00 61.65 1085 NH2 ARG A 489 24.480 90.013 5.866 1.00 62.45 1086 C ARG A 489 27.456 84.894 10.058 1.00 45.96 1087 O ARG A 489 27.501 85.912 10.746 1.00 45.86 1088 N HIS A 490 27.032 83.733 10.541 1.00 41.69 1089 CA HIS A 490 26.580 83.655 11.928 1.00 38.41 1090 CB HIS A 490 25.087 83.286 11.997 1.00 39.34 1091 CG HIS A 490 24.775 81.897 11.530 1.00 38.03 1092 CD2 HIS A 490 24.784 80.715 12.189 1.00 41.49 1093 ND1 HIS A 490 24.443 81.606 10.224 1.00 44.03 1094 CE1 HIS A 490 24.263 80.302 10.099 1.00 42.68 1095 NE2 HIS A 490 24.465 79.740 11.277 1.00 46.75 1096 C HIS A 490 27.382 82.679 12.778 1.00 37.56 1097 O HIS A 490 28.117 81.852 12.260 1.00 38.74 1098 N SER A 491 27.241 82.796 14.094 1.00 36.46 1099 CA SER A 491 27.926 81.906 15.021 1.00 35.63 1100 CB SER A 491 28.940 82.698 15.845 1.00 34.76 1101 OG SER A 491 29.650 81.849 16.726 1.00 51.24 1102 C SER A 491 26.888 81.245 15.935 1.00 32.46 1103 O SER A 491 26.122 81.928 16.618 1.00 34.26 1104 N THR A 492 26.868 79.919 15.946 1.00 30.35 1105 CA THR A 492 25.922 79.147 16.750 1.00 32.31 1106 CB THR A 492 25.104 78.179 15.837 1.00 33.20 1107 OG1 THR A 492 24.459 78.933 14.806 1.00 38.93 1108 CG2 THR A 492 24.046 77.415 16.622 1.00 30.28 1109 C THR A 492 26.639 78.328 17.835 1.00 32.83 1110 O THR A 492 27.638 77.670 17.565 1.00 34.30 1111 N THR A 493 26.118 78.360 19.058 1.00 32.82 1112 CA THR A 493 26.719 77.610 20.161 1.00 32.09 1113 CB THR A 493 26.254 78.151 21.530 1.00 27.96 1114 OG1 THR A 493 24.825 78.059 21.630 1.00 29.42 1115 CG2 THR A 493 26.680 79.600 21.694 1.00 21.13 1116 C THR A 493 26.336 76.131 20.067 1.00 34.06 1117 O THR A 493 25.436 75.770 19.317 1.00 31.49 1118 N CLN A 494 27.030 75.282 20.816 1.00 35.84 1119 CA GLN A 494 26.740 73.848 20.824 1.00 40.51 1120 CB CLN A 494 27.929 73.056 21.382 1.00 46.41 1121 CG GLN A 494 29.169 73.078 20.504 1.00 63.89 1122 CD GLN A 494 28.890 72.592 19.093 1.00 72.04 1123 OE1 CLN A 494 28.272 71.547 18.894 1.00 77.06 1124 NE2 CLN A 494 29.355 73.350 18.104 1.00 81.58 1125 C GLN A 494 25.512 73.596 21.691 1.00 39.51 1126 O CLN A 494 25.304 74.270 22.698 1.00 38.74 1127 N PRO A 495 24.676 72.623 21.305 1.00 38.63 1128 CD PRO A 495 24.687 71.849 20.051 1.00 37.82 1129 CA PRO A 495 23.480 72.330 22.100 1.00 39.10 1130 CB PRO A 495 22.889 71.124 21.391 1.00 37.94 1131 CG PRO A 495 23.255 71.388 19.954 1.00 43.34 1132 C PRO A 495 23.854 72.031 23.549 1.00 41.43 1133 O PRO A 495 24.838 71.346 23.808 1.00 42.40 1134 N ARG A 496 23.086 72.567 24.487 1.00 41.33 1135 CA ARG A 496 23.343 72.343 25.906 1.00 46.41 1136 CB ARG A 496 23.808 73.635 26.574 1.00 44.11 1137 CG ARG A 496 25.263 73.943 26.332 1.00 51.48 1138 CD ARG A 496 25.633 75.331 26.813 1.00 56.73 1139 NE ARG A 496 27.038 75.393 27.197 1.00 63.41 1140 CZ ARG A 496 27.507 74.984 28.373 1.00 59.61 1141 NH1 ARG A 496 26.683 74.489 29.286 1.00 60.71 1142 NH2 ARG A 496 28.804 75.066 28.634 1.00 67.27 1143 C ARG A 496 22.090 71.835 26.597 1.00 49.11 1144 O ARG A 496 20.989 72.303 26.318 1.00 48.52 1145 N LYS A 497 22.255 70.870 27.492 1.00 53.35 1146 CA LYS A 497 21.116 70.322 28.208 1.00 60.05 1147 CB LYS A 497 21.527 69.101 29.034 1.00 65.19 1148 CG LYS A 497 21.910 67.887 28.212 1.00 75.27 1149 CD LYS A 497 22.255 66.705 29.103 1.00 80.74 1150 CE LYS A 497 22.534 65.470 28.269 1.00 86.89 1151 NZ LYS A 497 22.854 64.278 29.103 1.00 91.84 1152 C LYS A 497 20.546 71.376 29.131 1.00 62.05 1153 O LYS A 497 21.184 72.391 29.403 1.00 61.50 1154 N THR A 498 19.335 71.135 29.604 1.00 66.47 1155 CA THR A 498 18.690 72.060 30.515 1.00 71.47 1156 CB THR A 498 17.417 72.654 29.893 1.00 73.54 1157 OG1 THR A 498 17.118 71.981 28.666 1.00 77.08 1158 CG2 THR A 498 17.619 74.120 29.609 1.00 75.50 1159 C THR A 498 18.339 71.319 31.794 1.00 72.65 1160 O THR A 498 18.850 70.223 32.037 1.00 72.18 1161 N ALA A 499 17.477 71.918 32.610 1.00 75.02 1162 CA ALA A 499 17.062 71.303 33.867 1.00 77.01 1163 CB ALA A 499 16.508 72.370 34.814 1.00 76.94 1164 C ALA A 499 16.009 70.224 33.607 1.00 77.96 1165 O ALA A 499 15.034 70.099 34.350 1.00 79.10 1166 N CLY A 500 16.214 69.443 32.552 1.00 78.37 1167 CA CLY A 500 15.273 68.390 32.217 1.00 78.64 1168 C CLY A 500 14.392 68.745 31.032 1.00 77.71 1169 O CLY A 500 13.741 67.878 30.447 1.00 78.53 1170 N SER A 501 14.390 70.021 30.661 1.00 76.72 1171 CA SER A 501 13.567 70.501 29.555 1.00 74.10 1172 CB SER A 501 13.017 71.893 29.899 1.00 79.09 1173 OG SER A 501 14.053 72.787 30.276 1.00 82.51 1174 C SER A 501 14.235 70.545 28.176 1.00 70.47 1175 O SER A 501 14.188 71.575 27.499 1.00 71.67 1176 N GLY A 502 14.849 69.435 27.761 1.00 64.36 1177 CA GLY A 502 15.484 69.369 26.447 1.00 55.25 1178 C GLY A 502 16.799 70.111 26.211 1.00 48.43 1179 O GLY A 502 17.669 70.155 27.081 1.00 47.45 1180 N PHE A 503 16.952 70.678 25.015 1.00 41.96 1181 CA PHE A 503 18.175 71.411 24.665 1.00 34.38 1182 CB PHE A 503 18.975 70.675 23.582 1.00 34.97 1183 CG PHE A 503 19.432 69.304 23.979 1.00 28.11 1184 CD1 PHE A 503 18.548 68.232 23.974 1.00 36.44 1185 CD2 PHE A 503 20.749 69.082 24.348 1.00 30.75 1186 CE1 PHE A 503 18.971 66.960 24.338 1.00 37.43 1187 CE2 PHE A 503 21.179 67.812 24.716 1.00 40.11 1188 CZ PHE A 503 20.289 66.750 24.709 1.00 37.06 1189 C PHE A 503 17.922 72.825 24.167 1.00 28.77 1190 O PHE A 503 16.816 73.176 23.756 1.00 28.23 1191 N PHE A 504 18.963 73.637 24.213 1.00 24.91 1192 CA PHE A 504 18.887 75.006 23.743 1.00 25.79 1193 CB PHE A 504 18.644 76.006 24.886 1.00 22.02 1194 CG PHE A 504 19.834 76.257 25.774 1.00 30.92 1195 CD1 PHE A 504 20.722 77.300 25.499 1.00 32.77 1196 CD2 PHE A 504 20.037 75.487 26.919 1.00 34.76 1197 CE1 PHE A 504 21.796 77.570 26.349 1.00 29.72 1198 CE2 PHE A 504 21.107 75.748 27.774 1.00 33.59 1199 CZ PHE A 504 21.987 76.799 27.480 1.00 34.51 1200 C PHE A 504 20.175 75.328 23.027 1.00 28.90 1201 O PHE A 504 21.222 74.751 23.317 1.00 26.02 1202 N VAL A 505 20.071 76.252 22.080 1.00 25.50 1203 CA VAL A 505 21.196 76.681 21.296 1.00 25.53 1204 CB VAL A 505 21.193 75.891 19.955 1.00 29.70 1205 CG1 VAL A 505 20.184 76.476 19.002 1.00 25.34 1206 CG2 VAL A 505 22.563 75.837 19.365 1.00 35.22 1207 C VAL A 505 21.015 78.196 21.092 1.00 26.24 1208 O VAL A 505 19.895 78.707 21.096 1.00 22.25 1209 N PHE A 506 22.125 78.913 20.950 1.00 28.62 1210 CA PHE A 506 22.093 80.361 20.754 1.00 25.84 1211 CB PHE A 506 22.769 81.061 21.935 1.00 29.19 1212 CG PHE A 506 22.789 82.547 21.827 1.00 35.82 1213 CD1 PHE A 506 21.630 83.286 22.030 1.00 42.42 1214 CD2 PHE A 506 23.961 83.213 21.500 1.00 42.16 1215 CE1 PHE A 506 21.644 84.671 21.910 1.00 44.85 1216 CE2 PHE A 506 23.982 84.591 21.376 1.00 41.56 1217 CZ PHE A 506 22.825 85.322 21.580 1.00 45.90 1218 C PHE A 506 22.844 80.719 19.473 1.00 23.92 1219 O PHE A 506 23.924 80.195 19.225 1.00 27.54 1220 N SER A 507 22.286 81.618 18.677 1.00 25.96 1221 CA SER A 507 22.925 82.041 17.432 1.00 25.75 1222 CB SER A 507 22.144 81.481 16.235 1.00 24.23 1223 OG SER A 507 22.674 81.957 15.012 1.00 33.35 1224 C SER A 507 23.027 83.574 17.364 1.00 25.49 1225 O SER A 507 22.070 84.284 17.648 1.00 25.61 1226 N ARG A 508 24.203 84.063 16.994 1.00 26.99 1227 CA ARG A 508 24.475 85.497 16.907 1.00 25.78 1228 CB AEG A 508 25.652 85.821 17.825 1.00 24.46 1229 CG ARG A 508 26.177 87.245 17.753 1.00 28.19 1230 CD ARG A 508 27.409 87.349 18.638 1.00 27.68 1231 NE ARG A 508 27.865 88.723 18.804 1.00 38.82 1232 CZ ARG A 508 28.641 89.355 17.933 1.00 40.66 1233 NE1 ARG A 508 29.046 88.726 16.840 1.00 39.61 1234 NH2 ARG A 508 29.007 90.613 18.151 1.00 40.23 1235 C ARG A 508 24.816 85.910 15.471 1.00 24.52 1236 O ARG A 508 25.594 85.234 14.810 1.00 24.88 1237 N LEU A 509 24.246 87.013 14.992 1.00 26.27 1238 CA LEU A 509 24.512 87.490 13.622 1.00 31.33 1239 CB LEU A 509 23.303 87.206 12.721 1.00 32.56 1240 CG LEU A 509 23.311 87.774 11.292 1.00 33.39 1241 CD1 LEU A 509 24.350 87.049 10.434 1.00 27.13 1242 CD2 LEU A 509 21.921 87.614 10.691 1.00 27.35 1243 C LEU A 509 24.830 88.988 13.550 1.00 33.20 1244 O LEU A 509 23.946 89.823 13.721 1.00 35.36 1245 N GLU A 510 26.091 89.330 13.286 1.00 33.43 1246 CA GLU A 510 26.479 90.735 13.182 1.00 37.45 1247 CB GLU A 510 28.002 90.880 13.305 1.00 38.70 1248 CG GLU A 510 28.548 90.352 14.629 1.00 53.61 1249 CD GLU A 510 30.009 90.722 14.897 1.00 62.03 1250 OE1 GLU A 510 30.877 90.439 14.042 1.00 65.31 1251 OE2 GLU A 510 30.288 91.290 15.976 1.00 63.62 1252 C GLU A 510 26.007 91.285 11.841 1.00 37.95 1253 O GLU A 510 26.187 90.635 10.808 1.00 35.84 1254 N VAL A 511 25.391 92.466 11.845 1.00 37.36 1255 CA VAL A 511 24.903 93.048 10.596 1.00 39.69 1256 CB VAL A 511 23.366 93.012 10.513 1.00 29.12 1257 CG1 VAL A 511 22.875 91.590 10.689 1.00 28.52 1258 CG2 VAL A 511 22.764 93.933 11.554 1.00 31.67 1259 C VAL A 511 25.357 94.490 10.392 1.00 45.51 1260 O VAL A 511 25.776 95.156 11.344 1.00 46.84 1261 N THR A 512 25.269 94.964 9.150 1.00 47.32 1262 CA THR A 512 25.673 96.326 8.813 1.00 51.20 1263 CE THR A 512 25.922 96.471 7.304 1.00 49.91 1264 OG1 THR A 512 24.723 96.142 6.592 1.00 46.57 1265 CG2 THR A 512 27.046 95.544 6.858 1.00 49.02 1266 C THR A 512 24.585 97.312 9.213 1.00 54.77 1267 O THR A 512 23.467 96.909 9.520 1.00 54.38 1268 N ARG A 513 24.916 98.602 9.206 1.00 56.48 1269 CA ARG A 513 23.955 99.642 9.565 1.00 56.58 1270 CB ARG A 513 24.609 101.026 9.503 1.00 61.58 1271 CG ARG A 513 24.030 102.030 10.489 1.00 67.62 1272 CD ARG A 513 22.566 102.306 10.221 1.00 75.58 1273 NE ARG A 513 21.857 102.737 11.422 1.00 83.06 1274 CZ ARG A 513 20.572 103.081 11.448 1.00 86.37 1275 NH1 ARG A 513 19.856 103.049 10.336 1.00 88.41 1276 NH2 ARG A 513 19.998 103.446 12.585 1.00 87.87 1277 C ARG A 513 22.783 99.603 8.600 1.00 55.15 1278 O ARG A 513 21.639 99.856 8.983 1.00 55.55 1279 N ALA A 514 23.076 99.281 7.345 1.00 55.02 1280 CA ALA A 514 22.055 99.214 6.308 1.00 53.96 1281 CB ALA A 514 22.715 98.972 4.961 1.00 53.56 1282 C ALA A 514 21.015 98.128 6.595 1.00 54.12 1283 O ALA A 514 19.819 98.413 6.681 1.00 54.41 1284 N GLU A 515 21.464 96.884 6.736 1.00 54.63 1285 CA GLU A 515 20.535 95.798 7.011 1.00 54.64 1286 CB GLU A 515 21.225 94.434 6.862 1.00 58.15 1287 CG GLU A 515 22.668 94.392 7.331 1.00 64.48 1288 CD GLU A 515 23.379 93.107 6.926 1.00 65.38 1289 OE1 GLU A 515 23.183 92.643 5.784 1.00 66.84 1290 OE2 GLU A 515 24.149 92.563 7.741 1.00 68.35 1291 C GLU A 515 19.929 95.956 8.395 1.00 54.36 1292 O GLU A 515 18.897 95.360 8.694 1.00 51.06 1293 N TRP A 516 20.563 96.769 9.237 1.00 55.85 1294 CA TRP A 516 20.043 97.015 10.576 1.00 57.10 1295 CB TRP A 516 21.062 97.755 11.447 1.00 58.50 1296 CG TRP A 516 20.726 97.650 12.906 1.00 67.12 1297 CD2 TRP A 516 20.128 98.660 13.726 1.00 68.04 1298 CE2 TRP A 516 19.915 98.091 14.999 1.00 71.07 1299 CE3 TRP A 516 19.751 99.992 13.507 1.00 74.06 1300 CD1 TRP A 516 20.851 96.541 13.697 1.00 67.58 1301 NE1 TRP A 516 20.364 96.797 14.954 1.00 68.75 1302 CZ2 TRP A 516 19.337 98.807 16.052 1.00 75.59 1303 CZ3 TRP A 516 19.175 100.705 14.558 1.00 76.50 1304 CH2 TRP A 516 18.975 100.109 15.813 1.00 76.13 1305 C TRP A 516 18.772 97.854 10.452 1.00 57.68 1306 O TRP A 516 17.909 97.825 11.327 1.00 57.71 1307 N GLU A 517 18.665 98.604 9.357 1.00 58.53 1308 CA GLU A 517 17.487 99.427 9.092 1.00 60.83 1309 CE GLU A 517 17.758 100.381 7.921 1.00 65.68 1310 CG GLU A 517 18.237 101.768 8.325 1.00 77.69 1311 CD GLU A 517 17.213 102.522 9.168 1.00 86.61 1312 OE1 GLU A 517 16.066 102.036 9.301 1.00 92.24 1313 OE2 GLU A 517 17.550 103.605 9.696 1.00 89.43 1314 C GLU A 517 16.277 98.547 8.755 1.00 58.89 1315 O GLU A 517 15.135 98.871 9.088 1.00 56.98 1316 N ALA A 518 16.537 97.430 8.084 1.00 58.33 1317 CA ALA A 518 15.479 96.503 7.702 1.00 54.78 1318 CB ALA A 518 15.595 96.178 6.220 1.00 55.11 1319 C ALA A 518 15.597 95.227 8.540 1.00 53.56 1320 O ALA A 518 15.375 94.120 8.045 1.00 52.54 1321 N LYS A 519 15.919 95.381 9.819 1.00 51.73 1322 CA LYS A 519 16.092 94.217 10.671 1.00 52.62 1323 CB LYS A 519 16.719 94.617 12.004 1.00 52.68 1324 CG LYS A 519 15.808 95.347 12.954 1.00 53.71 1325 CD LYS A 519 16.631 95.904 14.103 1.00 61.43 1326 CE LYS A 519 15.781 96.701 15.064 1.00 65.64 1327 NE LYS A 519 16.642 97.460 16.002 1.00 74.93 1328 C LYS A 519 14.814 93.440 10.915 1.00 52.55 1329 O LYS A 519 14.857 92.287 11.339 1.00 49.84 1330 N ASP A 520 13.680 94.067 10.638 1.00 54.27 1331 CA ASP A 520 12.381 93.424 10.820 1.00 55.54 1332 CB ASP A 520 11.263 94.454 10.669 1.00 65.40 1333 CG ASP A 520 11.743 95.878 10.904 1.00 75.80 1334 OD1 ASP A 520 12.217 96.174 12.024 1.00 83.22 1335 OD2 ASP A 520 11.652 96.700 9.964 1.00 77.87 1336 C ASP A 520 12.212 92.345 9.754 1.00 53.46 1337 O ASP A 520 11.319 91.500 9.843 1.00 51.37 1338 N GLU A 521 13.079 92.383 8.747 1.00 50.72 1339 CA GLU A 521 13.016 91.422 7.658 1.00 50.66 1340 CE GLU A 521 13.427 92.093 6.342 1.00 54.68 1341 CO GLU A 521 12.408 93.090 5.799 1.00 61.75 1342 CD GLU A 521 12.961 93.937 4.670 1.00 68.36 1343 OE1 GLU A 521 13.463 93.368 3.678 1.00 70.14 1344 OE2 GLU A 521 12.892 95.181 4.773 1.00 75.93 1345 C GLU A 521 13.869 90.182 7.885 1.00 46.52 1346 O GLU A 521 13.743 89.208 7.148 1.00 47.21 1347 N PHE A 522 14.734 90.214 8.893 1.00 42.97 1348 CA PHE A 522 15.589 89.069 9.181 1.00 38.46 1349 CB PHE A 522 16.848 89.509 9.915 1.00 37.28 1350 CG PHE A 522 17.846 90.180 9.024 1.00 42.52 1351 CD1 PHE A 522 17.675 91.510 8.646 1.00 44.12 1352 CD2 PHE A 522 18.929 89.467 8.508 1.00 40.14 1353 CE1 PHE A 522 18.564 92.126 7.762 1.00 48.02 1354 CE2 PHE A 522 19.825 90.072 7.623 1.00 42.77 1355 CZ PHE A 522 19.640 91.408 7.248 1.00 41.32 1356 C PHE A 522 14.852 88.006 9.970 1.00 36.02 1357 O PHE A 522 14.126 88.308 10.918 1.00 37.87 1358 N ILE A 523 15.042 86.758 9.561 1.00 32.13 1359 CA ILE A 523 14.376 85.626 10.187 1.00 31.74 1360 CB ILE A 523 13.392 84.966 9.192 1.00 36.58 1361 CG2 ILE A 523 12.711 83.751 9.838 1.00 38.36 1362 CG1 ILE A 523 12.367 86.000 8.714 1.00 39.38 1363 CD1 ILE A 523 11.517 85.514 7.564 1.00 40.35 1364 C ILE A 523 15.356 84.559 10.670 1.00 30.51 1365 O ILE A 523 16.369 84.294 10.034 1.00 29.34 1366 N CYS A 524 15.046 83.949 11.802 1.00 28.73 1367 CA CYS A 524 15.879 82.898 12.351 1.00 27.60 1368 C CYS A 524 15.081 81.635 12.136 1.00 27.54 1369 O CYS A 524 13.933 81.567 12.555 1.00 28.72 1370 CB CYS A 524 16.096 83.123 13.849 1.00 26.75 1371 SG CYS A 524 16.999 81.777 14.689 1.00 36.31 1372 N ARG A 525 15.675 80.636 11.497 1.00 28.42 1373 CA ARG A 525 14.966 79.400 11.226 1.00 28.35 1374 CB ARG A 525 14.780 79.229 9.720 1.00 34.16 1375 CG ARG A 525 14.120 77.912 9.331 1.00 39.75 1376 CD ARG A 525 13.508 77.996 7.937 1.00 48.43 1377 NE ARG A 525 14.483 77.825 6.874 1.00 52.97 1378 CZ ARG A 525 14.242 78.108 5.598 1.00 58.72 1379 NH1 ARG A 525 13.054 78.580 5.233 1.00 55.56 1380 NH2 ARG A 525 15.190 77.930 4.686 1.00 55.90 1381 C ARG A 525 15.673 78.184 11.783 1.00 28.14 1382 O ARG A 525 16.889 78.055 11.691 1.00 28.95 1383 N ALA A 526 14.892 77.283 12.357 1.00 25.82 1384 CA ALA A 526 15.440 76.082 12.930 1.00 25.90 1385 CB ALA A 526 15.056 75.986 14.409 1.00 28.82 1386 C ALA A 526 14.871 74.903 12.169 1.00 27.38 1387 O ALA A 526 13.690 74.899 11.847 1.00 24.32 1388 N VAL A 527 15.718 73.924 11.855 1.00 24.37 1389 CA VAL A 527 15.266 72.727 11.177 1.00 24.12 1390 CB VAL A 527 16.054 72.434 9.899 1.00 24.30 1391 CG1 VAL A 527 15.637 71.090 9.338 1.00 26.10 1392 CG2 VAL A 527 15.796 73.517 8.876 1.00 30.97 1393 C VAL A 527 15.523 71.646 12.198 1.00 26.78 1394 O VAL A 527 16.631 71.522 12.725 1.00 25.10 1395 N HIS A 528 14.497 70.857 12.470 1.00 26.18 1396 CA HIS A 528 14.585 69.829 13.484 1.00 29.17 1397 CB HIS A 528 14.413 70.490 14.879 1.00 28.69 1398 CC HIS A 528 14.409 69.522 16.028 1.00 30.83 1399 CD2 HIS A 528 13.456 68.661 16.461 1.00 30.29 1400 ND1 HIS A 528 15.504 69.318 16.842 1.00 30.55 1401 CE1 HIS A 528 15.228 68.367 17.719 1.00 28.76 1402 NE2 HIS A 528 13.992 67.950 17.507 1.00 23.82 1403 C HIS A 528 13.498 68.782 13.230 1.00 31.62 1404 O HIS A 528 12.387 69.096 12.788 1.00 30.62 1405 N GLU A 529 13.834 67.539 13.543 1.00 34.89 1406 CA GLU A 529 12.949 66.400 13.347 1.00 41.27 1407 CB GLU A 529 13.640 65.129 13.843 1.00 46.90 1408 CG GLU A 529 12.721 63.908 13.872 1.00 61.52 1409 CD GLU A 529 13.184 62.836 14.852 1.00 68.52 1410 OE1 GLU A 529 12.433 61.860 15.064 1.00 68.05 1411 OE2 GLU A 529 14.294 62.969 15.413 1.00 73.22 1412 C GLU A 529 11.565 66.476 13.996 1.00 42.79 1413 O GLU A 529 10.578 66.069 13.381 1.00 42.08 1414 N ALA A 530 11.502 66.978 15.232 1.00 43.28 1415 CA ALA A 530 10.250 67.061 15.987 1.00 44.89 1416 CB ALA A 530 10.546 67.183 17.472 1.00 42.67 1417 C ALA A 530 9.263 68.142 15.582 1.00 47.12 1418 O ALA A 530 8.126 68.137 16.048 1.00 47.05 1419 N ALA A 531 9.684 69.071 14.732 1.00 50.02 1420 CA ALA A 531 8.792 70.130 14.280 1.00 54.71 1421 CB ALA A 531 9.602 71.233 13.621 1.00 52.38 1422 C ALA A 531 7.787 69.519 13.292 1.00 59.71 1423 O ALA A 531 7.784 69.835 12.102 1.00 57.91 1424 N SER A 532 6.936 68.642 13.825 1.00 66.39 1425 CA SER A 532 5.911 67.899 13.078 1.00 71.61 1426 CB SER A 532 4.570 67.949 13.828 1.00 75.15 1427 OG SER A 532 4.190 69.274 14.168 1.00 81.74 1428 C SER A 532 5.681 68.198 11.595 1.00 73.08 1429 O SER A 532 5.855 67.307 10.757 1.00 75.98 1430 N PRO A 533 5.279 69.433 11.236 1.00 72.21 1431 CD PRO A 533 4.769 70.589 11.998 1.00 72.93 1432 CA PRO A 533 5.076 69.644 9.801 1.00 69.88 1433 CB PRO A 533 3.913 70.617 9.775 1.00 69.60 1434 CG PRO A 533 4.278 71.537 10.895 1.00 71.96 1435 C PRO A 533 6.317 70.212 9.113 1.00 67.12 1436 O PRO A 533 6.820 71.269 9.500 1.00 67.77 1437 N SER A 534 6.802 69.499 8.103 1.00 62.96 1438 CA SER A 534 7.967 69.917 7.331 1.00 56.20 1439 CB SER A 534 7.609 71.137 6.479 1.00 57.74 1440 OG SER A 534 6.985 72.137 7.262 1.00 67.85 1441 C SER A 534 9.258 70.194 8.111 1.00 49.03 1442 O SER A 534 10.176 70.811 7.576 1.00 47.21 1443 N OLN A 535 9.322 69.742 9.363 1.00 42.33 1444 CA OLN A 535 10.504 69.896 10.204 1.00 38.93 1445 CB OLN A 535 11.588 68.887 9.784 1.00 32.30 1446 CG OLN A 535 11.212 67.419 9.972 1.00 35.25 1447 CD GLN A 535 10.074 66.981 9.076 1.00 41.01 1448 OE1 OLN A 535 10.112 67.172 7.861 1.00 43.29 1449 NE2 GLN A 535 9.055 66.380 9.669 1.00 47.79 1450 C OLN A 535 11.115 71.290 10.209 1.00 37.85 1451 O OLN A 535 12.335 71.432 10.281 1.00 36.76 1452 N THR A 536 10.280 72.317 10.147 1.00 37.28 1453 CA THR A 536 10.795 73.675 10.145 1.00 39.00 1454 CB THR A 536 10.752 74.281 8.734 1.00 41.53 1455 OG1 THR A 536 11.256 73.333 7.786 1.00 46.75 1456 CG2 THR A 536 11.613 75.524 8.676 1.00 39.44 1457 C THR A 536 10.014 74.584 11.072 1.00 38.42 1458 O THR A 536 8.806 74.452 11.205 1.00 43.26 1459 N VAL A 537 10.723 75.495 11.726 1.00 37.42 1460 CA VAL A 537 10.138 76.469 12.632 1.00 32.52 1461 CB VAL A 537 10.134 75.981 14.110 1.00 36.29 1462 CG1 VAL A 537 9.452 77.020 14.986 1.00 35.71 1463 C02 VAL A 537 9.395 74.669 14.241 1.00 43.42 1464 C VAL A 537 11.006 77.724 12.538 1.00 31.41 1465 O VAL A 537 12.231 77.654 12.665 1.00 31.67 1466 N OLN A 538 10.381 78.874 12.313 1.00 27.91 1467 CA GLN A 538 11.148 80.104 12.183 1.00 29.41 1468 CB GLN A 538 11.464 80.369 10.708 1.00 29.17 1469 CG GLN A 538 10.237 80.635 9.849 1.00 29.81 1470 CD GLN A 538 10.617 80.890 8.409 1.00 29.58 1471 OE1 GLN A 538 11.424 80.157 7.833 1.00 37.40 1472 NE2 GLN A 538 10.041 81.924 7.815 1.00 32.13 1473 C GLN A 538 10.407 81.296 12.744 1.00 31.40 1474 O GLN A 538 9.189 81.286 12.844 1.00 33.62 1475 N ARG A 539 11.151 82.333 13.098 1.00 31.64 1476 CA ARG A 539 10.537 83.534 13.619 1.00 34.86 1477 CB ARG A 539 10.480 83.480 15.145 1.00 41.64 1478 CG ARG A 539 9.522 84.477 15.762 1.00 48.95 1479 CD ARG A 539 8.755 83.804 16.884 1.00 59.63 1480 NE ARG A 539 8.205 82.533 16.420 1.00 74.02 1481 CZ ARG A 539 7.506 81.691 17.173 1.00 82.05 1482 NH1 ARG A 539 7.259 81.977 18.447 1.00 87.03 1483 NH2 ARG A 539 7.053 80.560 16.646 1.00 85.40 1484 C ARG A 539 11.311 84.760 13.178 1.00 34.74 1485 O ARG A 539 12.541 84.767 13.190 1.00 37.29 1486 N ALA A 540 10.580 85.794 12.772 1.00 34.85 1487 CA ALA A 540 11.192 87.039 12.344 1.00 34.24 1488 CB ALA A 540 10.175 87.891 11.628 1.00 35.02 1489 C ALA A 540 11.700 87.754 13.587 1.00 35.51 1490 O ALA A 540 11.205 87.518 14.695 1.00 30.77 1491 N VAL A 541 12.704 88.604 13.408 1.00 36.19 1492 CA VAL A 541 13.274 89.349 14.520 1.00 42.85 1493 CB VAL A 541 14.428 90.265 14.038 1.00 43.71 1494 CG1 VAL A 541 14.744 91.316 15.084 1.00 48.75 1495 CG2 VAL A 541 15.665 89.433 13.749 1.00 43.59 1496 C VAL A 541 12.181 90.194 15.178 1.00 48.00 1497 O VAL A 541 11.587 91.063 14.536 1.00 44.96 1498 N SER A 542 11.906 89.927 16.451 1.00 53.41 1499 CA SER A 542 10.883 90.686 17.152 1.00 61.94 1500 CB SER A 542 10.532 90.036 18.494 1.00 62.96 1501 OG SER A 542 11.596 90.138 19.421 1.00 69.91 1502 C SER A 542 11.437 92.083 17.372 1.00 65.98 1503 O SER A 542 12.628 92.253 17.634 1.00 67.12 1504 N VAL A 543 10.571 93.080 17.249 1.00 70.21 1505 CA VAL A 543 10.975 94.466 17.421 1.00 74.63 1506 CB VAL A 543 11.300 95.121 16.058 1.00 78.23 1507 CG1 VAL A 543 11.713 96.574 16.260 1.00 79.65 1508 CC2 VAL A 543 12.409 94.344 15.359 1.00 79.80 1509 C VAL A 543 9.871 95.259 18.111 1.00 75.67 1510 O VAL A 543 8.974 95.753 17.396 1.00 77.58 1511 OXT VAL A 543 9.907 95.360 19.356 1.00 74.95 1512 C1 NAG A 2 39.866 71.246 15.298 1.00 97.60 1513 O1 NAG A 2 39.913 72.355 16.125 1.00 99.81 1514 C2 NAG A 2 38.452 71.095 14.687 1.00 96.75 1515 N2 NAG A 2 38.075 72.305 13.989 1.00 98.55 1516 C7 NAG A 2 38.040 72.336 12.660 1.00 101.24 1517 O7 NAG A 2 38.381 71.38S 11.956 1.00 100.19 1518 C8 NAG A 2 37.567 73.623 12.006 1.00 100.76 1519 C3 NAG A 2 37.394 70.819 1S.772 1.00 96.21 1520 O3 NAG A 2 36.138 70.S2S 1S.162 1.00 95.30 1521 C4 NAG A 2 37.840 69.634 16.642 1.00 94.75 1522 O4 NAG A 2 36.924 69.444 17.72S 1.00 91.92 1523 C5 NAG A 2 39.273 69.896 17.179 1.00 95.52 1524 O5 NAG A 2 40.204 70.093 16.083 1.00 96.34 1525 C6 NAG A 2 39.775 68.727 17.999 1.00 96.13 1526 O6 NAG A 2 39.723 67.507 17.266 1.00 99.34 1527 OH2 TIP A 1 24.621 77.330 12.183 1.00 50.26 1528 OH2 TIP A 2 17.289 54.802 2.062 1.00 49.71 1529 OH2 TIP A 3 10.654 89.058 −3.198 1.00 62.73 1530 OH2 TIP A 4 22.344 80.875 7.156 1.00 44.66 1531 OE2 TIP A 5 27.537 65.331 9.249 1.00 53.56 1532 OH2 TIP A 6 26.192 96.403 20.749 1.00 44.98 1533 OH2 TIP A 7 8.855 79.202 17.894 1.00 44.08 1534 OH2 TIP A 8 16.591 66.982 14.521 1.00 40.39 1535 OH2 TIP A 9 24.434 65.928 6.674 1.00 40.49 1536 OH2 TIP A 10 27.385 88.484 9.939 1.00 46.89 1537 OH2 TIP A 11 28.304 87.357 13.183 1.00 50.51 1538 OH2 TIP A 12 28.907 78.522 14.088 1.00 50.17 1539 OH2 TIP A 13 47.570 70.510 13.386 1.00 54.70 1540 OH2 TIP A 14 23.814 76.382 23.745 1.00 44.57 1541 OH2 TIP A 15 22.971 61.676 0.664 1.00 50.94 1542 OH2 TIP A 16 19.616 104.062 18.276 1.00 56.21 1543 OH2 TIP A 17 30.294 75.010 30.820 1.00 59.52 1544 OH2 TIP A 18 10.090 82.420 4.828 1.00 55.58 1545 OH2 TIP A 19 45.243 73.089 9.124 1.00 66.56 1546 OH2 TIP A 20 46.743 70.603 11.012 1.00 63.77 1547 OH2 TIP A 21 29.058 92.561 8.613 1.00 62.34 1548 OH2 TIP A 22 26.556 59.226 16.825 1.00 54.44 1549 OH2 TIP A 23 26.041 54.669 2.219 1.00 52.42 1550 OH2 TIP A 24 34.966 68.214 16.774 1.00 60.14 1551 OH2 TIP A 25 20.048 55.636 12.052 1.00 48.11 1552 OH2 TIP A 26 28.830 86.081 15.665 1.00 45.10 1553 OH2 TIP A 27 34.158 69.085 18.975 1.00 59.32 1554 OH2 TIP A 28 28.875 47.094 5.425 1.00 53.61 1555 OH2 TIP A 29 26.558 67.506 3.036 1.00 60.13 1556 OH2 TIP A 30 38.399 52.730 18.974 1.00 56.34 1557 OH2 TIP A 31 23.500 72.144 10.139 1.00 58.14 1558 OH2 TIP A 32 34.771 64.807 3.542 1.00 50.57 1559 OH2 TIP A 33 24.268 95.724 3.944 1.00 56.48 1560 OH2 TIP A 34 27.690 78.824 11.826 1.00 60.64 1561 OH2 TIP A 35 49.321 73.518 9.173 1.00 56.75 1562 OH2 TIP A 36 20.391 63.685 13.114 1.00 52.49 1563 OH2 TIP A 37 25.216 70.518 28.590 1.00 56.17 1564 OH2 TIP A 38 42.408 48.356 24.205 1.00 57.49 1565 OH2 TIP A 39 29.180 99.267 16.299 1.00 59.27 1566 OH2 TIP A 40 14.998 75.915 2.509 1.00 55.17 1567 OH2 TIP A 41 25.941 69.212 22.056 1.00 55.25 1568 OH2 TIP A 42 11.307 86.566 17.528 1.00 50.93 1569 OH2 TIP A 43 26.577 64.924 15.413 1.00 58.05 1570 OH2 TIP A 44 9.305 75.672 24.091 1.00 63.22 1571 OH2 TIP A 45 31.263 91.102 9.512 1.00 59.76 1572 OH2 TIP A 46 29.116 71.553 15.523 1.00 61.09 1573 OH2 TIP A 47 20.286 50.431 1.295 1.00 58.75 1574 OH2 TIP A 48 39.170 57.553 3.300 1.00 59.73 1575 OH2 TIP A 49 8.842 71.660 23.296 1.00 53.77 1576 OH2 TIP A 50 12.559 48.527 9.562 1.00 59.31 1577 OH2 TIP A 51 28.206 76.115 14.977 1.00 56.85 1578 OH2 TIP A 52 8.825 77.060 27.183 1.00 60.05 1579 OH2 TIP A 53 32.649 60.706 17.690 1.00 57.10 1580 OH2 TIP A 54 49.662 60.238 13.997 1.00 60.54 1581 OH2 TIP A 55 30.363 57.461 17.811 1.00 62.47 1582 OH2 TIP A 56 24.541 106.634 19.860 1.00 64.33 1583 OH2 TIP A 57 11.412 70.168 26.131 1.00 52.42 1584 OH2 TIP A 58 10.025 88.314 3.596 1.00 60.20 1585 OH2 TIP A 59 22.043 63.628 26.199 1.00 59.26 1586 OH2 TIP A 60 46.414 76.131 6.439 1.00 62.09 1587 OH2 TIP A 61 22.767 54.070 3.523 1.00 65.16 1588 OH2 TIP A 62 14.610 78.959 1.837 1.00 59.85 1589 OH2 TIP A 63 18.102 59.201 0.758 1.00 56.88 1590 OH2 TIP A 64 29.616 80.265 4.265 1.00 53.06 1591 OH2 TIP A 65 18.383 97.407 19.064 1.00 60.26 1592 OH2 TIP A 66 16.855 77.568 2.254 1.00 59.03 1593 OH2 TIP A 67 32.757 64.887 12.306 1.00 54.95 1594 OH2 TIP A 68 27.226 97.417 12.532 1.00 57.65 1595 OH2 TIP A 69 16.812 67.479 30.053 1.00 59.41 1596 OH2 TIP A 70 12.053 64.929 3.775 1.00 62.27 1597 OH2 TIP A 71 36.626 74.187 14.978 1.00 55.86 1598 OH2 TIP A 72 33.116 54.343 0.777 1.00 59.39 1599 OH2 TIP A 73 21.701 75.116 6.786 1.00 59.25 1600 OH2 TIP A 74 33.920 50.039 9.248 1.00 53.17 1601 OH2 TIP A 75 10.687 52.377 4.811 1.00 65.55 1602 OH2 TIP A 76 41.791 50.133 21.910 1.00 62.05 1603 OH2 TIP A 77 38.603 74.281 16.682 1.00 57.87 1604 OH2 TIP A 78 11.460 76.303 28.686 1.00 58.31 1605 OH2 TIP A 79 22.506 95.718 17.568 1.00 53.97 1606 OH2 TIP A 80 20.912 49.812 13.914 1.00 54.45 1607 OH2 TIP A 81 21.594 91.198 3.704 1.00 60.50 1608 OH2 TIP A 82 5.956 84.199 15.573 1.00 54.25 1609 OH2 TIP A 83 6.295 66.853 17.967 1.00 58.03 1610 OH2 TIP A 84 13.965 68.899 −2.314 1.00 61.54 1611 OH2 TIP A 85 32.379 52.416 −8.311 1.00 71.84 1612 OH2 TIP A 86 48.425 50.638 14.271 1.00 59.92 1613 OH2 TIP A 87 10.680 67.805 5.635 1.00 55.82 1614 OH2 TIP A 88 36.880 58.553 1.670 1.00 57.31 1615 OH2 TIP A 89 16.870 52.214 1.693 1.00 58.45 1616 OH2 TIP A 90 25.408 92.634 4.035 1.00 58.03 1617 OH2 TIP A 91 13.095 80.378 22.328 1.00 50.36 1618 OH2 TIP A 92 29.763 48.629 0.935 1.00 57.19 1619 OH2 TIP A 93 48.144 52.717 5.484 1.00 62.27 1620 OH2 TIP A 94 32.716 83.953 9.514 1.00 61.49 1621 OH2 TIP A 95 50.245 51.781 10.104 1.00 66.72 1622 OH2 TIP A 96 19.486 103.622 14.976 1.00 62.93 1623 OH2 TIP A 97 16.771 101.927 12.421 1.00 59.08 1624 OH2 TIP A 98 53.390 55.312 11.504 1.00 66.54 1625 OH2 TIP A 99 50.837 51.731 13.291 1.00 64.16 1626 OH2 TIP A 100 23.981 65.804 −2.209 1.00 59.09 1627 OH2 TIP A 101 23.552 78.063 7.649 1.00 59.99 1628 OH2 TIP A 102 2.205 69.469 16.152 1.00 63.48 1629 OH2 TIP A 103 28.886 49.557 15.035 1.00 60.94 1630 OH2 TIP A 104 16.467 73.762 27.029 1.00 57.13 1631 OH2 TIP A 105 12.719 56.573 17.218 1.00 67.01 1632 OH2 TIP A 106 35.645 52.940 2.917 1.00 61.12 1633 OH2 TIP A 107 21.697 47.608 11.251 1.00 62.98 1634 OH2 TIP A 108 29.875 69.867 19.761 1.00 63.30 1635 OH2 TIP A 109 7.022 65.025 20.275 1.00 57.78 1636 OH2 TIP A 110 23.672 57.957 18.156 1.00 65.34 1637 OH2 TIP A 111 18.442 100.288 19.662 1.00 56.09 1638 OH2 TIP A 112 17.274 55.759 23.904 1.00 62.75 1639 OH2 TIP A 113 12.468 99.002 11.775 1.00 58.88 1640 OH2 TIP A 114 4.947 78.508 15.926 1.00 63.28 1641 OH2 TIP A 115 51.851 63.576 7.665 1.00 65.61 1642 OH2 TIP A 116 28.686 55.061 19.178 1.00 60.98 1643 OH2 TIP A 117 13.344 58.062 13.444 1.00 60.98 1644 OH2 TIP A 118 31.348 100.434 17.891 1.00 58.25 1645 OH2 TIP A 119 33.355 67.383 15.181 1.00 55.39 1646 OH2 TIP A 120 50.364 73.348 11.901 1.00 56.80 1647 OH2 TIP A 121 48.002 72.930 13.297 1.00 61.15 1648 OH2 TIP A 122 8.619 87.814 −3.671 1.00 55.82 1649 OH2 TIP A 123 28.580 65.220 7.059 1.00 45.14 1650 OH2 TIP A 124 17.490 63.562 13.375 1.00 55.49 1651 OH2 TIP A 125 50.105 70.842 12.277 1.00 66.22 1652 OH2 TIP A 126 28.516 67.863 5.456 1.00 57.00 1653 OH2 TIP A 127 7.299 75.901 18.432 1.00 57.60 1654 OH2 TIP A 128 16.230 56.580 0.876 1.00 56.82 1655 OH2 TIP A 129 29.715 52.741 21.104 1.00 62.05 1656 OH2 TIP A 130 46.391 75.590 10.503 1.00 66.31 1657 OH2 TIP A 131 8.623 74.686 21.869 1.00 57.71 1658 OH2 TIP A 132 25.877 65.684 −0.527 1.00 61.64 1659 OH2 TIP A 133 48.195 61.492 2.382 1.00 61.06 1660 OH2 TIP A 134 26.143 95.737 23.267 1.00 61.78 1661 OH2 TIP A 135 19.283 66.683 28.340 1.00 57.35 1662 OH2 TIP A 136 23.744 74.738 11.921 1.00 54.03 1663 OH2 TIP A 137 34.653 51.896 −6.794 1.00 64.00 1664 OH2 TIP A 138 23.762 64.741 24.873 1.00 65.85 1665 OH2 TIP A 139 9.472 67.784 26.691 1.00 60.91 1666 OH2 TIP A 140 31.126 79.895 13.795 1.00 61.62 1667 OH2 TIP A 141 51.302 75.595 10.454 1.00 62.13 1668 OH2 TIP A 142 25.624 94.976 18.923 1.00 58.14 1669 OH2 TIP A 143 46.215 76.102 4.024 1.00 61.05 1670 OH2 TIP A 144 14.705 65.280 31.014 1.00 55.65 1671 OH2 TIP A 145 39.069 49.876 20.322 1.00 64.64 1672 OH2 TIP A 146 10.862 54.941 15.417 1.00 61.54 1673 OH2 TIP A 147 20.183 101.944 22.268 1.00 59.07 1674 OH2 TIP A 148 29.707 89.335 8.858 1.00 60.79 1675 OH2 TIP A 149 10.193 73.823 5.510 1.00 57.59 1676 OH2 TIP A 150 29.352 51.313 −6.490 1.00 63.92 1677 OH2 TIP A 151 25.999 72.109 30.307 1.00 62.67 1678 OH2 TIP A 152 10.844 86.445 −4.018 1.00 68.07 1679 OH2 TIP A 153 30.550 70.355 12.969 1.00 61.87 1680 OH2 TIP A 154 28.953 49.265 12.349 1.00 66.95 1681 OH2 TIP A 155 10.816 50.012 8.484 1.00 59.56 1682 OH2 TIP A 156 27.343 69.536 30.284 1.00 59.20 1683 OH2 TIP A 157 48.276 50.311 10.430 1.00 67.18 1684 OH2 TIP A 158 9.916 67.356 2.963 1.00 59.37 1685 OH2 TIP A 159 24.834 107.006 22.307 1.00 65.79 1686 OH2 TIP A 160 15.746 59.001 13.607 1.00 58.89 1687 OH2 TIP A 161 31.698 74.365 32.777 1.00 59.68 1688 OH2 TIP A 162 21.890 56.335 −1.064 1.00 63.91 1689 OH2 TIP A 163 14.286 93.107 19.563 1.00 58.95 1690 OH2 TIP A 164 23.710 75.161 5.470 1.00 64.19 1691 OH2 TIP A 165 24.206 72.021 7.712 1.00 55.30 1692 OH2 TIP A 166 20.559 81.972 −0.663 1.00 55.04 1693 OH2 TIP A 167 28.070 68.574 17.772 1.00 61.56 1694 OH2 TIP A 168 57.914 63.409 6.737 1.00 63.55 1695 OH2 TIP A 169 18.340 57.211 25.770 1.00 62.46 1696 OH2 TIP A 170 26.782 106.710 18.895 1.00 61.28 1697 OH2 TIP A 171 28.254 75.284 31.745 1.00 59.15 1698 OH2 TIP A 172 46.877 48.708 12.388 1.00 66.69 1699 OH2 TIP A 173 15.777 67.027 −3.922 1.00 60.64 1700 OH2 TIP A 174 32.197 49.900 17.143 1.00 64.56 1701 OH2 TIP A 175 23.440 103.469 17.348 1.00 59.77 1702 OH2 TIP A 176 30.137 56.948 21.224 1.00 61.95 1703 OH2 TIP A 177 26.468 91.670 1.313 1.00 63.68 1704 OH2 TIP A 178 25.828 56.552 19.074 1.00 62.71 1705 OH2 TIP A 179 34.582 54.727 20.637 1.00 64.40 1706 OH2 TIP A 180 17.987 105.822 18.202 1.00 64.94 1707 OH2 TIP A 181 6.122 68.884 20.390 1.00 60.70 1708 OH2 TIP A 182 8.806 49.867 4.420 1.00 62.42 1709 OH2 TIP A 183 27.312 72.638 16.534 1.00 65.26 1710 OH2 TIP A 184 31.069 55.528 19.225 1.00 58.49 1711 OH2 TIP A 185 25.301 101.534 21.383 1.00 66.38 1712 OH2 TIP A 186 22.607 53.815 1.063 1.00 66.62 1713 OH2 TIP A 187 16.147 98.913 21.300 1.00 63.72 1714 OH2 TIP A 188 17.776 102.185 18.290 1.00 62.49 1715 OH2 TIP A 189 31.779 47.168 4.361 1.00 63.23 1716 OH2 TIP A 190 16.083 101.996 14.898 1.00 65.15 1717 OH2 TIP A 191 36.208 68.938 20.199 1.00 63.27 1718 OH2 TIP A 192 36.586 54.580 0.794 1.00 61.81 1719 OH2 TIP A 193 32.810 70.773 20.047 1.00 59.78 1720 OH2 TIP A 194 7.956 66.621 5.340 1.00 60.91 1721 OH2 TIP A 195 16.254 80.162 0.421 1.00 61.51 1722 CB VAL B 336 45.054 59.383 30.496 1.00 63.58 1723 CG1 VAL B 336 45.744 60.010 31.695 1.00 64.78 1724 CG2 VAL B 336 44.712 57.923 30.765 1.00 68.51 1725 C VAL B 336 44.164 61.555 29.666 1.00 61.62 1726 O VAL B 336 45.201 61.720 29.026 1.00 64.02 1727 N VAL B 336 42.976 59.439 29.128 1.00 59.58 1728 CA VAL B 336 43.773 60.162 30.157 1.00 61.95 1729 N SER B 337 43.338 62.554 29.963 1.00 59.54 1730 CA SER B 337 43.618 63.921 29.536 1.00 57.94 1731 CB SER B 337 42.531 64.396 28.575 1.00 56.70 1732 OG SER B 337 41.253 64.019 29.047 1.00 65.28 1733 C SER B 337 43.767 64.903 30.700 1.00 56.67 1734 O SER B 337 43.366 64.613 31.832 1.00 56.61 1735 N ALA B 338 44.355 66.061 30.413 1.00 52.92 1736 CA ALA B 338 44.589 67.079 31.429 1.00 51.01 1737 CB ALA B 338 46.038 67.024 31.884 1.00 50.96 1738 C ALA B 338 44.252 68.480 30.934 1.00 50.95 1739 O ALA B 338 44.396 68.784 29.748 1.00 53.16 1740 N TYR B 339 43.795 69.328 31.850 1.00 47.68 1741 CA TYR B 339 43.431 70.697 31.508 1.00 48.08 1742 CB TYR B 339 41.925 70.790 31.203 1.00 50.34 1743 CG TYR B 339 41.382 69.708 30.283 1.00 58.74 1744 CD1 TYR B 339 41.179 68.404 30.745 1.00 60.22 1745 CE1 TYR B 339 40.705 67.401 29.895 1.00 64.78 1746 CD2 TYR B 339 41.094 69.984 28.947 1.00 60.49 1747 CE2 TYR B 339 40.620 68.992 28.088 1.00 63.00 1748 CZ TYR B 339 40.428 67.700 28.567 1.00 67.92 1749 OH TYR B 339 39.974 66.709 27.718 1.00 68.47 1750 C TYR B 339 43.785 71.646 32.663 1.00 45.49 1751 O TYR B 339 43.556 71.338 33.833 1.00 43.52 1752 N LEU B 340 44.362 72.792 32.325 1.00 44.01 1753 CA LEU B 340 44.728 73.784 33.324 1.00 42.54 1754 CB LEU B 340 46.237 74.050 33.284 1.00 39.07 1755 CG LEU B 340 46.850 74.948 34.370 1.00 39.58 1756 CD1 LEU B 340 46.526 74.402 35.751 1.00 28.76 1757 CD2 LEU B 340 48.364 75.029 34.177 1.00 35.57 1758 C LEU B 340 43.955 75.043 32.966 1.00 42.53 1759 O LEU B 340 43.962 75.462 31.814 1.00 43.25 1760 N SER B 341 43.276 75.643 33.940 1.00 42.42 1761 CA SER B 341 42.497 76.848 33.675 1.00 40.32 1762 CB SER B 341 41.014 76.603 33.995 1.00 41.30 1763 OG SER B 341 40.842 76.184 35.336 1.00 45.86 1764 C SER B 341 42.994 78.037 34.466 1.00 38.67 1765 O SER B 341 43.552 77.893 35.541 1.00 42.94 1766 N ARG B 342 42.777 79.222 33.923 1.00 37.60 1767 CA ARG B 342 43.186 80.445 34.580 1.00 35.91 1768 CB ARG B 342 43.241 81.574 33.548 1.00 36.67 1769 OG ARG B 342 44.285 81.346 32.454 1.00 39.89 1770 CD ARG B 342 44.278 82.459 31.421 1.00 42.31 1771 NE ARG B 342 43.066 82.415 30.610 1.00 45.87 1772 CZ ARG B 342 42.870 81.595 29.580 1.00 52.30 1773 NE1 ARG B 342 43.810 80.739 29.205 1.00 56.74 1774 NH2 ARG B 342 41.715 81.619 28.932 1.00 58.22 1775 C ARG B 342 42.191 80.768 35.702 1.00 34.19 1776 O ARG B 342 41.150 80.124 35.822 1.00 34.44 1777 N PRO B 343 42.499 81.763 36.545 1.00 31.22 1778 CD PRO B 343 43.729 82.572 36.606 1.00 34.08 1779 CA PRO B 343 41.576 82.114 37.634 1.00 33.86 1780 CB PRO B 343 42.356 83.163 38.437 1.00 32.10 1781 CG PRO B 343 43.811 82.902 38.078 1.00 37.07 1782 C PRO B 343 40.277 82.703 37.085 1.00 32.54 1783 O PRO B 343 40.281 83.330 36.028 1.00 35.02 1784 N SER B 344 39.168 82.510 37.789 1.00 33.04 1785 CA SER B 344 37.913 83.085 37.322 1.00 34.74 1786 CB SER B 344 36.703 82.428 38.005 1.00 35.18 1787 OG SER B 344 36.507 82.937 39.308 1.00 35.70 1788 C SER B 344 37.972 84.562 37.685 1.00 35.17 1789 O SER B 344 38.468 84.931 38.751 1.00 32.53 1790 N PRO B 345 37.506 85.438 36.787 1.00 35.98 1791 CD PRO B 345 37.180 85.223 35.364 1.00 36.93 1792 CA PRO B 345 37.544 86.869 37.105 1.00 34.79 1793 CB PRO B 345 36.870 87.503 35.888 1.00 30.45 1794 CG PRO B 345 37.379 86.612 34.769 1.00 30.91 1795 C PRO B 345 36.861 87.215 38.433 1.00 34.13 1796 O PRO B 345 37.283 88.129 39.137 1.00 34.14 1797 N PHE B 346 35.817 86.476 38.791 1.00 31.57 1798 CA PHE B 346 35.134 86.752 40.041 1.00 33.19 1799 CB PHE B 346 33.876 85.889 40.165 1.00 37.49 1800 CG PHE B 346 33.206 85.984 41.505 1.00 38.65 1801 CD1 PHE B 346 32.621 87.168 41.922 1.00 42.62 1802 CD2 PHE B 346 33.159 84.881 42.353 1.00 43.21 1803 CE1 PHE B 346 31.992 87.256 43.167 1.00 41.72 1804 CE2 PHE B 346 32.531 84.957 43.604 1.00 49.00 1805 CZ PHE B 346 31.946 86.148 44.009 1.00 42.82 1806 C PHE B 346 36.070 86.501 41.233 1.00 33.37 1807 O PHE B 346 36.143 87.316 42.152 1.00 33.52 1808 N ASP B 347 36.790 85.384 41.216 1.00 32.94 1809 CA ASP B 347 37.709 85.067 42.308 1.00 33.61 1810 CB ASP B 347 38.242 83.638 42.173 1.00 29.68 1811 CG ASP B 347 37.222 82.589 42.559 1.00 35.85 1812 OD1 ASP B 347 37.516 81.386 42.382 1.00 42.71 1813 OD2 ASP B 347 36.128 82.954 43.044 1.00 50.58 1814 C ASP B 347 38.882 86.036 42.338 1.00 33.62 1815 O ASP B 347 39.381 86.399 43.401 1.00 30.10 1816 N LEU B 348 39.312 86.463 41.160 1.00 34.23 1817 CA LEU B 348 40.437 87.374 41.046 1.00 38.75 1818 CB LEU B 348 40.964 87.340 39.604 1.00 38.06 1819 CG LEU B 348 42.165 88.237 39.289 1.00 43.84 1820 CD1 LEU B 348 43.357 87.861 40.190 1.00 39.77 1821 CD2 LEU B 348 42.536 88.090 37.809 1.00 43.35 1822 C LEU B 348 40.161 88.837 41.455 1.00 39.57 1823 O LEU B 348 40.979 89.454 42.141 1.00 38.51 1824 N PHE B 349 39.017 89.386 41.043 1.00 40.41 1825 CA PHE B 349 38.699 90.791 41.338 1.00 42.87 1826 CB PHE B 349 38.236 91.489 40.060 1.00 39.59 1827 CG PHE B 349 39.217 91.392 38.937 1.00 37.95 1828 CD1 PHE B 349 38.951 90.596 37.832 1.00 36.40 1829 CD2 PHE B 349 40.419 92.083 38.995 1.00 40.49 1830 CE1 PHE B 349 39.874 90.484 36.795 1.00 39.63 1831 CE2 PHE B 349 41.353 91.981 37.965 1.00 38.12 1832 CZ PHE B 349 41.080 91.182 36.863 1.00 41.86 1833 C PHE B 349 37.704 91.128 42.446 1.00 44.67 1834 O PHE B 349 37.827 92.167 43.099 1.00 47.25 1835 N ILE B 350 36.705 90.286 42.650 1.00 46.06 1836 CA ILE B 350 35.729 90.573 43.683 1.00 50.35 1837 CB ILE B 350 34.330 90.052 43.287 1.00 50.30 1838 CG2 ILE B 350 33.284 90.603 44.236 1.00 51.91 1839 CG1 ILE B 350 34.007 90.454 41.839 1.00 51.78 1840 CD1 ILE B 350 34.234 91.915 41.520 1.00 45.73 1841 C ILE B 350 36.179 89.906 44.973 1.00 51.95 1842 O ILE B 350 36.454 90.572 45.970 1.00 52.71 1843 N ARG B 351 36.281 88.584 44.927 1.00 53.39 1844 CA ARG B 351 36.691 87.787 46.069 1.00 54.67 1845 CB ARG B 351 36.541 86.310 45.707 1.00 59.14 1846 CG ARG B 351 36.063 85.414 46.833 1.00 64.87 1847 CD ARG B 351 35.127 84.346 46.292 1.00 66.51 1848 NE ARG B 351 35.034 83.195 47.180 1.00 73.42 1849 CZ ARG B 351 36.027 82.337 47.383 1.00 78.26 1850 NH1 ARG B 351 37.183 82.506 46.756 1.00 81.30 1851 NH2 ARG B 351 35.867 81.312 48.211 1.00 79.63 1852 C ARG B 351 38.132 88.092 46.484 1.00 53.92 1853 O ARG B 351 38.456 88.090 47.667 1.00 53.66 1854 N LYS B 352 38.988 88.352 45.502 1.00 53.41 1855 CA LYS B 352 40.400 88.658 45.740 1.00 53.02 1856 CB LYS B 352 40.547 89.821 46.725 1.00 54.25 1857 CG LYS B 352 39.848 91.094 46.286 1.00 64.61 1858 CD LYS B 352 40.158 92.234 47.246 1.00 71.92 1859 CE LYS B 352 39.190 93.398 47.086 1.00 76.75 1860 NZ LYS B 352 37.807 93.027 47.505 1.00 82.42 1861 C LYS B 352 41.217 87.470 46.253 1.00 51.14 1862 O LYS B 352 42.183 87.655 46.991 1.00 51.55 1863 N SER B 353 40.828 86.259 45.863 1.00 47.69 1864 CA SER B 353 41.533 85.048 46.268 1.00 45.50 1865 CB SER B 353 40.882 84.446 47.518 1.00 50.28 1866 OG SER B 353 39.542 84.062 47.271 1.00 63.45 1867 C SER B 353 41.465 84.072 45.094 1.00 40.39 1868 O SER B 353 40.710 83.102 45.105 1.00 40.20 1869 N PRO B 354 42.271 84.332 44.055 1.00 36.74 1870 CD PRO B 354 43.262 85.412 44.061 1.00 36.52 1871 CA PRO B 354 42.376 83.557 42.817 1.00 34.20 1872 CB PRO B 354 43.283 84.418 41.937 1.00 31.70 1873 CG PRO B 354 43.340 85.730 42.628 1.00 40.26 1874 C PRO B 354 42.964 82.167 42.979 1.00 32.13 1875 O PRO B 354 43.829 81.945 43.817 1.00 28.54 1876 N THR B 355 42.489 81.241 42.158 1.00 30.96 1877 CA THR B 355 42.999 79.882 42.164 1.00 31.86 1878 CB THR B 355 42.099 78.908 42.979 1.00 32.67 1879 OG1 THR B 355 40.823 78.794 42.348 1.00 34.86 1880 CG2 THR B 355 41.894 79.406 44.401 1.00 34.90 1881 C THR B 355 43.052 79.379 40.726 1.00 33.38 1882 O THR B 355 42.361 79.897 39.840 1.00 32.61 1883 N ILE B 356 43.909 78.403 40.482 1.00 32.83 1884 CA ILE B 356 43.959 77.807 39.165 1.00 33.21 1885 CB ILE B 356 45.297 78.062 38.434 1.00 34.88 1886 CG2 ILE B 356 45.458 79.562 38.190 1.00 34.84 1887 CG1 ILE B 356 46.465 77.502 39.240 1.00 37.26 1888 CD1 ILE B 356 47.843 77.791 38.611 1.00 38.06 1889 C ILE B 356 43.745 76.335 39.461 1.00 32.48 1890 O ILE B 356 44.037 75.861 40.564 1.00 30.30 1891 N THR B 357 43.236 75.609 38.478 1.00 33.59 1892 CA THR B 357 42.929 74.211 38.694 1.00 32.83 1893 CB THR B 357 41.384 74.025 38.857 1.00 37.46 1894 OG1 THR B 357 40.955 74.615 40.091 1.00 35.11 1895 CG2 THR B 357 41.001 72.553 38.842 1.00 40.13 1896 C THR B 357 43.420 73.326 37.570 1.00 34.22 1897 O THR B 357 43.222 73.609 36.384 1.00 33.99 1898 N CYS B 358 44.045 72.231 37.966 1.00 34.04 1899 CA CYS B 358 44.563 71.256 37.032 1.00 36.90 1900 C CYS B 358 43.573 70.104 37.101 1.00 36.26 1901 O CYS B 358 43.412 69.497 38.156 1.00 35.68 1902 CB CYS B 358 45.930 70.791 37.507 1.00 39.83 1903 SG CYS B 358 46.881 69.819 36.302 1.00 52.73 1904 N LEU B 359 42.908 69.820 35.988 1.00 38.57 1905 CA LEU B 359 41.921 68.751 35.922 1.00 42.35 1906 CB LEU B 359 40.615 69.273 35.304 1.00 42.11 1907 CG LEU B 359 39.572 68.227 34.881 1.00 48.42 1908 CD1 LEU B 359 39.146 67.379 36.073 1.00 49.46 1909 CD2 LEU B 359 38.370 68.934 34.269 1.00 48.09 1910 C LEU B 359 42.437 67.589 35.095 1.00 45.39 1911 O LEU B 359 42.794 67.766 33.935 1.00 48.73 1912 N VAL B 360 42.479 66.405 35.693 1.00 47.72 1913 CA VAL B 360 42.931 65.205 34.996 1.00 51.87 1914 CB VAL B 360 44.075 64.514 35.765 1.00 52.99 1915 CG1 VAL B 360 44.490 63.235 35.051 1.00 51.29 1916 CG2 VAL B 360 45.252 65.456 35.890 1.00 52.42 1917 C VAL B 360 41.767 64.221 34.874 1.00 55.21 1918 O VAL B 360 41.063 63.966 35.853 1.00 56.01 1919 N VAL B 361 41.558 63.680 33.677 1.00 57.47 1920 CA VAL B 361 40.479 62.718 33.448 1.00 61.75 1921 CB VAL B 361 39.447 63.248 32.425 1.00 58.91 1922 CG1 VAL B 361 38.368 62.211 32.187 1.00 56.98 1923 CG2 VAL B 361 38.826 64.530 32.934 1.00 54.49 1924 C VAL B 361 41.045 61.403 32.923 1.00 66.78 1925 O VAL B 361 41.836 61.392 31.981 1.00 67.30 1926 N ASP B 362 40.641 60.299 33.544 1.00 72.35 1927 CA ASP B 362 41.100 58.969 33.145 1.00 79.16 1928 CB ASP B 362 41.775 58.266 34.331 1.00 83.66 1929 CG ASP B 362 42.511 56.997 33.924 1.00 87.40 1930 OD1 ASP B 362 42.317 56.529 32.780 1.00 91.40 1931 OD2 ASP B 362 43.282 56.462 34.752 1.00 87.33 1932 C ASP B 362 39.896 58.156 32.676 1.00 82.84 1933 O ASP B 362 39.113 57.663 33.493 1.00 84.14 1934 N ALA B 363 39.751 58.022 31.360 1.00 85.70 1935 CA ALA B 363 38.636 57.281 30.775 1.00 89.05 1936 CB ALA B 363 38.830 57.154 29.270 1.00 90.18 1937 C ALA B 363 38.458 55.899 31.401 1.00 91.80 1938 O ALA B 363 37.354 55.357 31.409 1.00 92.23 1939 N ALA B 364 39.544 55.337 31.926 1.00 94.23 1940 CA ALA B 364 39.515 54.022 32.564 1.00 97.42 1941 CB ALA B 364 39.441 52.932 31.506 1.00 96.05 1942 C ALA B 364 40.772 53.845 33.413 1.00 100.00 1943 O ALA B 364 41.885 53.833 32.887 1.00 101.29 1944 N PRO B 365 40.612 53.715 34.741 1.00 101.76 1945 CD PRO B 365 39.442 54.193 35.503 1.00 101.62 1946 CA PRO B 365 41.764 53.547 35.632 1.00 103.14 1947 CB PRO B 365 41.486 54.578 36.706 1.00 103.27 1948 CG PRO B 365 40.006 54.372 36.917 1.00 103.12 1949 C PRO B 365 41.919 52.144 36.228 1.00 104.03 1950 O PRO B 365 42.228 51.181 35.521 1.00 104.47 1951 N ALA B 366 41.716 52.064 37.543 1.00 104.37 1952 CA ALA B 366 41.807 50.824 38.307 1.00 104.87 1953 CB ALA B 366 40.895 49.761 37.687 1.00 105.36 1954 C ALA B 366 43.230 50.281 38.435 1.00 104.90 1955 O ALA B 366 43.492 49.139 38.055 1.00 105.14 1956 N LYS B 367 44.148 51.086 38.971 1.00 104.05 1957 CA LYS B 367 45.523 50.618 39.128 1.00 103.07 1958 CB LYS B 367 46.061 50.117 37.785 1.00 103.33 1959 CG LYS B 367 46.194 51.189 36.717 1.00 102.12 1960 CD LYS B 367 46.962 50.649 35.528 1.00 103.99 1961 CE LYS B 367 47.229 51.724 34.496 1.00 103.83 1962 NZ LYS B 367 48.056 51.183 33.386 1.00 105.88 1963 C LYS B 367 46.554 51.576 39.727 1.00 102.12 1964 O LYS B 367 47.653 51.712 39.185 1.00 103.05 1965 N GLY B 368 46.228 52.235 40.835 1.00 99.91 1966 CA OLY B 368 47.212 53.120 41.436 1.00 96.70 1967 C GLY B 368 46.800 54.521 41.845 1.00 94.03 1968 O GLY B 368 45.651 54.771 42.209 1.00 94.76 1969 N ALA B 369 47.761 55.438 41.787 1.00 90.44 1970 CA ALA B 369 47.534 56.828 42.165 1.00 86.18 1971 CB ALA B 369 48.292 57.140 43.455 1.00 86.97 1972 C ALA B 369 47.961 57.792 41.062 1.00 82.79 1973 O ALA B 369 48.773 57.451 40.203 1.00 83.46 1974 N VAL B 370 47.407 59.000 41.099 1.00 78.82 1975 CA VAL B 370 47.719 60.033 40.115 1.00 73.44 1976 CB VAL B 370 46.468 60.439 39.323 1.00 71.37 1977 CG1 VAL B 370 46.837 61.455 38.260 1.00 68.72 1978 CG2 VAL B 370 45.831 59.212 38.696 1.00 66.32 1979 C VAL B 370 48.254 61.253 40.848 1.00 71.19 1980 O VAL B 370 47.581 61.797 41.717 1.00 70.77 1981 N ASN B 371 49.462 61.687 40.495 1.00 69.11 1982 CA ASN B 371 50.069 62.831 41.164 1.00 67.35 1983 CB ASN B 371 51.462 62.455 41.670 1.00 68.95 1984 CG ASN B 371 51.432 61.270 42.602 1.00 73.37 1985 OD1 ASN B 371 50.772 61.301 43.641 1.00 76.52 1986 ND2 ASN B 371 52.146 60.213 42.237 1.00 76.06 1987 C ASN B 371 50.159 64.109 40.334 1.00 65.35 1988 O ASN B 371 50.454 64.084 39.136 1.00 63.63 1989 N LEU B 372 49.892 65.227 41.000 1.00 63.51 1990 CA LEU B 372 49.949 66.540 40.379 1.00 60.50 1991 CB LEU B 372 48.573 67.214 40.395 1.00 60.09 1992 CG LEU B 372 47.430 66.461 39.714 1.00 61.37 1993 CD1 LEU B 372 46.196 67.335 39.688 1.00 63.12 1994 CD2 LEU B 372 47.829 66.083 38.309 1.00 62.53 1995 C LEU B 372 50.942 67.380 41.164 1.00 57.54 1996 O LEU B 372 50.824 67.531 42.380 1.00 58.06 1997 N THR B 373 51.926 67.919 40.458 1.00 54.64 1998 CA THR B 373 52.952 68.745 41.074 1.00 52.59 1999 CB THR B 373 54.346 68.175 40.786 1.00 54.37 2000 OG1 THR B 373 54.383 66.801 41.191 1.00 60.15 2001 CG2 THR B 373 55.409 68.955 41.545 1.00 57.66 2002 C THR B 373 52.878 70.156 40.509 1.00 48.12 2003 O THR B 373 52.803 70.337 39.297 1.00 46.78 2004 N TRP B 374 52.895 71.150 41.391 1.00 45.42 2005 CA TRP B 374 52.833 72.543 40.971 1.00 44.33 2006 CB TRP B 374 51.838 73.340 41.823 1.00 40.42 2007 CG TRP B 374 50.417 72.936 41.658 1.00 41.22 2008 CD2 TRP B 374 49.510 73.385 40.643 1.00 35.68 2009 CE2 TRP B 374 48.271 72.759 40.881 1.00 31.67 2010 CE3 TRP B 374 49.628 74.258 39.555 1.00 35.08 2011 CD1 TRP B 374 49.712 72.077 42.448 1.00 38.77 2012 NE1 TRP B 374 48.420 71.966 41.988 1.00 37.27 2013 CZ2 TRP B 374 47.153 72.979 40.073 1.00 32.53 2014 CZ3 TRP B 374 48.516 74.479 38.748 1.00 36.03 2015 CH2 TRP B 374 47.296 73.840 39.013 1.00 33.34 2016 C TRP B 374 54.195 73.215 41.078 1.00 44.84 2017 O TRP B 374 55.019 72.842 41.914 1.00 43.54 2018 N SER B 375 54.419 74.205 40.218 1.00 44.41 2019 CA SER B 375 55.660 74.967 40.213 1.00 45.63 2020 CB SER B 375 56.800 74.168 39.565 1.00 47.59 2021 OG SER B 375 56.662 74.088 38.157 1.00 49.42 2022 C SER B 375 55.488 76.292 39.482 1.00 45.23 2023 O SER B 375 54.609 76.438 38.629 1.00 46.27 2024 N ARG B 376 56.323 77.259 39.843 1.00 42.63 2025 CA ARG B 376 56.293 78.567 39.218 1.00 41.96 2026 CB ARG B 376 56.337 79.676 40.266 1.00 43.72 2027 CG ARG B 376 55.142 79.745 41.199 1.00 40.62 2028 CD ARG B 376 54.907 81.195 41.580 1.00 41.72 2029 NE ARG B 376 55.132 81.457 42.990 1.00 52.53 2030 CZ ARG B 376 55.295 82.671 43.501 1.00 52.81 2031 NH1 ARG B 376 55.265 83.741 42.714 1.00 51.46 2032 NH2 ARG B 376 55.472 82.819 44.807 1.00 56.61 2033 C ARG B 376 57.518 78.680 38.325 1.00 39.96 2034 O ARG B 376 58.629 78.382 38.745 1.00 40.84 2035 N ALA B 377 57.315 79.097 37.086 1.00 41.64 2036 CA ALA B 377 58.423 79.250 36.154 1.00 41.34 2037 CB ALA B 377 57.920 79.895 34.873 1.00 33.50 2038 C ALA B 377 59.544 80.098 36.775 1.00 41.22 2039 O ALA B 377 60.712 79.915 36.452 1.00 41.04 2040 N SER B 378 59.179 81.008 37.677 1.00 40.92 2041 CA SER B 378 60.149 81.881 38.327 1.00 42.71 2042 CB SER B 378 59.461 83.109 38.915 1.00 44.29 2043 OG SER B 378 58.733 82.758 40.080 1.00 42.78 2044 C SER B 378 60.894 81.180 39.442 1.00 43.58 2045 O SER B 378 61.809 81.749 40.022 1.00 44.22 2046 N GLY B 379 60.483 79.954 39.751 1.00 43.82 2047 CA GLY B 379 61.137 79.191 40.796 1.00 45.23 2048 C GLY B 379 60.683 79.540 42.199 1.00 48.43 2049 O GLY B 379 61.038 78.853 43.157 1.00 47.67 2050 N LYS B 380 59.901 80.605 42.337 1.00 50.04 2051 CA LYS B 380 59.423 80.997 43.653 1.00 52.22 2052 CB LYS B 380 58.732 82.362 43.591 1.00 54.82 2053 CG LYS B 380 59.721 83.504 43.454 1.00 63.15 2054 CD LYS B 380 59.072 84.866 43.634 1.00 70.67 2055 CE LYS B 380 60.133 85.960 43.645 1.00 75.50 2056 NZ LYS B 380 59.549 87.325 43.746 1.00 80.58 2057 C LYS B 380 58.493 79.945 44.249 1.00 52.26 2058 O LYS B 380 57.944 79.105 43.535 1.00 49.96 2059 N PRO B 381 58.315 79.974 45.578 1.00 53.55 2060 CD PRO B 381 58.943 80.906 46.529 1.00 54.43 2061 CA PRO B 381 57.453 79.016 46.282 1.00 54.97 2062 CB PRO B 381 57.652 79.388 47.755 1.00 57.06 2063 CG PRO B 381 58.989 80.081 47.773 1.00 59.10 2064 C PRO B 381 55.974 79.068 45.893 1.00 54.14 2065 O PRO B 381 55.422 80.143 45.633 1.00 55.04 2066 N VAL B 382 55.344 77.899 45.849 1.00 52.78 2067 CA VAL B 382 53.920 77.799 45.554 1.00 53.97 2068 CB VAL B 382 53.603 76.709 44.489 1.00 54.50 2069 CG1 VAL B 382 54.348 77.005 43.204 1.00 56.74 2070 CG2 VAL B 382 53.955 75.319 45.022 1.00 46.72 2071 C VAL B 382 53.262 77.398 46.874 1.00 54.10 2072 O VAL B 382 53.865 76.690 47.683 1.00 53.38 2073 N ASN B 383 52.034 77.848 47.089 1.00 53.55 2074 CA ASN B 383 51.311 77.527 48.310 1.00 54.35 2075 CB ASN B 383 50.115 78.465 48.470 1.00 60.43 2076 CG ASN B 383 50.513 79.923 48.471 1.00 67.43 2077 OD1 ASN B 383 49.710 80.794 48.137 1.00 75.26 2078 ND2 ASN B 383 51.755 80.201 48.856 1.00 72.99 2079 C ASN B 383 50.821 76.080 48.318 1.00 52.64 2080 O ASN B 383 51.082 75.308 47.393 1.00 50.26 2081 N HIS B 384 50.107 75.721 49.376 1.00 51.74 2082 CA HIS B 384 49.562 74.375 49.515 1.00 51.28 2083 CB HIS B 384 49.220 74.101 50.979 1.00 59.06 2084 CG HIS B 384 50.421 73.943 51.861 1.00 65.42 2085 CD2 HIS B 384 50.873 74.688 52.896 1.00 72.26 2086 ND1 HIS B 384 51.316 72.906 51.715 1.00 70.87 2087 CE1 HIS B 384 52.270 73.019 52.623 1.00 76.58 2088 NE2 HIS B 384 52.024 74.093 53.353 1.00 77.95 2089 C HIS B 384 48.306 74.238 48.655 1.00 47.99 2090 O HIS B 384 47.455 75.122 48.644 1.00 45.37 2091 N SER B 385 48.187 73.127 47.944 1.00 45.57 2092 CA SER B 385 47.036 72.926 47.085 1.00 45.69 2093 CB SER B 385 47.503 72.466 45.695 1.00 41.19 2094 OG SER B 385 48.315 71.301 45.762 1.00 41.34 2095 C SER B 385 46.002 71.946 47.660 1.00 44.94 2096 O SER B 385 46.287 71.187 48.582 1.00 41.64 2097 N THR B 386 44.795 71.997 47.107 1.00 45.73 2098 CA THR B 386 43.702 71.133 47.521 1.00 46.08 2099 CB THR B 386 42.409 71.930 47.737 1.00 47.42 2100 OG1 THR B 386 42.576 72.825 48.844 1.00 50.45 2101 CG2 THR B 386 41.253 70.985 48.025 1.00 51.73 2102 C THR B 386 43.468 70.113 46.419 1.00 46.45 2103 O THR B 386 43.359 70.471 45.247 1.00 47.06 2104 N ARG B 387 43.394 68.846 46.808 1.00 46.33 2105 CA ARG B 387 43.190 67.751 45.872 1.00 46.50 2106 CB ARG B 387 44.310 66.726 46.070 1.00 48.08 2107 CG ARG B 387 44.234 65.514 45.167 1.00 54.89 2108 CD ARG B 387 45.119 64.392 45.695 1.00 59.67 2109 NE ARG B 387 44.932 63.162 44.935 1.00 63.12 2110 CZ ARG B 387 45.650 62.825 43.870 1.00 65.65 2111 NH1 ARG B 387 46.618 63.629 43.449 1.00 67.29 2112 NH2 ARG B 387 45.385 61.701 43.211 1.00 63.40 2113 C ARG B 387 41.814 67.083 46.054 1.00 46.30 2114 O ARG B 387 41.361 66.867 47.179 1.00 44.30 2115 N LYS B 388 41.159 66.766 44.938 1.00 45.70 2116 CA LYS B 388 39.851 66.111 44.960 1.00 44.68 2117 CB LYS B 388 38.748 67.121 44.634 1.00 46.84 2118 CG LYS B 388 38.669 68.263 45.624 1.00 56.94 2119 CD LYS B 388 37.921 69.450 45.046 1.00 58.62 2120 CE LYS B 388 38.293 70.717 45.791 1.00 61.92 2121 NZ LYS B 388 37.744 71.924 45.123 1.00 70.07 2122 C LYS B 388 39.802 64.954 43.957 1.00 44.52 2123 O LYS B 388 40.221 65.098 42.806 1.00 40.60 2124 N GLU B 389 39.296 63.807 44.411 1.00 47.26 2125 CA GLU B 389 39.176 62.599 43.582 1.00 50.72 2126 CB GLU B 389 40.069 61.486 44.135 1.00 54.88 2127 CG GLU B 389 41.559 61.752 44.061 1.00 67.37 2128 CD GLU B 389 42.375 60.621 44.664 1.00 75.83 2129 OE1 GLU B 389 41.858 59.484 44.736 1.00 79.33 2130 OE2 GLU B 389 43.538 60.862 45.056 1.00 80.70 2131 C GLU B 389 37.729 62.090 43.549 1.00 51.11 2132 O GLU B 389 37.090 61.956 44.596 1.00 48.28 2133 N ALA B 390 37.218 61.786 42.359 1.00 52.07 2134 CA ALA B 390 35.845 61.303 42.232 1.00 56.84 2135 CB ALA B 390 34.888 62.480 42.128 1.00 53.86 2136 C ALA B 390 35.643 60.371 41.042 1.00 60.96 2137 O ALA B 390 36.285 60.515 40.002 1.00 61.14 2138 N ALA B 391 34.727 59.421 41.204 1.00 65.61 2139 CA ALA B 391 34.413 58.449 40.162 1.00 68.46 2140 CB ALA B 391 35.264 57.202 40.339 1.00 71.73 2141 C ALA B 391 32.939 58.082 40.234 1.00 70.37 2142 O ALA B 391 32.139 58.524 39.412 1.00 72.17 2143 N LEU B 397 37.390 58.285 36.020 1.00 60.70 2144 CA LEU B 397 37.949 58.914 37.210 1.00 61.36 2145 CB LEU B 397 39.142 58.111 37.725 1.00 64.28 2146 CG LEU B 397 39.864 58.746 38.920 1.00 65.19 2147 CD1 LEU B 397 38.930 58.798 40.119 1.00 65.40 2148 CD2 LEU B 397 41.115 57.948 39.256 1.00 68.57 2149 C LEU B 397 38.389 60.359 36.981 1.00 61.24 2150 O LEU B 397 39.115 60.666 36.036 1.00 62.11 2151 N THR B 398 37.946 61.240 37.867 1.00 59.83 2152 CA THR B 398 38.291 62.650 37.795 1.00 58.04 2153 CB THR B 398 37.028 63.539 37.837 1.00 58.72 2154 OG1 THR B 398 36.322 63.429 36.594 1.00 64.28 2155 CG2 THR B 398 37.403 64.992 38.077 1.00 61.55 2156 C THR B 398 39.199 63.027 38.965 1.00 55.72 2157 O THR B 398 39.005 62.579 40.100 1.00 55.02 2158 N VAL B 399 40.199 63.848 38.678 1.00 52.38 2159 CA VAL B 399 41.127 64.303 39.698 1.00 49.13 2160 CB VAL B 399 42.421 63.457 39.709 1.00 51.57 2161 CG1 VAL B 399 43.388 64.006 40.737 1.00 52.00 2162 CG2 VAL B 399 42.100 62.010 40.032 1.00 55.81 2163 C VAL B 399 41.507 65.753 39.457 1.00 46.27 2164 O VAL B 399 41.951 66.122 38.368 1.00 43.17 2165 N THR B 400 41.311 66.585 40.470 1.00 44.56 2166 CA THR B 400 41.685 67.981 40.342 1.00 43.39 2167 CB THR B 400 40.460 68.931 40.271 1.00 41.43 2168 OG1 THR B 400 39.806 68.972 41.543 1.00 48.65 2169 CG2 THR B 400 39.480 68.474 39.211 1.00 38.93 2170 C THR B 400 42.541 68.426 41.516 1.00 40.85 2171 O THR B 400 42.506 67.849 42.606 1.00 35.85 2172 N SER B 401 43.333 69.454 41.253 1.00 39.13 2173 CA SER B 401 44.183 70.058 42.253 1.00 37.93 2174 CB SER B 401 45.656 69.715 42.021 1.00 40.15 2175 OG SER B 401 46.458 70.310 43.031 1.00 44.51 2176 C SER B 401 43.978 71.546 42.056 1.00 36.16 2177 O SER B 401 44.139 72.048 40.947 1.00 36.19 2178 N THR B 402 43.611 72.238 43.125 1.00 32.94 2179 CA THR B 402 43.396 73.669 43.061 1.00 32.35 2180 CB THR B 402 42.022 74.022 43.617 1.00 33.13 2181 OG1 THR B 402 41.041 73.321 42.854 1.00 34.46 2182 CG2 THR B 402 41.755 75.514 43.523 1.00 33.71 2183 C THR B 402 44.483 74.378 43.857 1.00 31.66 2184 O THR B 402 44.714 74.088 45.036 1.00 26.99 2185 N LEU B 403 45.141 75.318 43.187 1.00 32.16 2186 CA LEU B 403 46.230 76.074 43.781 1.00 32.46 2187 CB LEU B 403 47.477 75.952 42.895 1.00 34.12 2188 CG LEU B 403 48.762 76.680 43.306 1.00 34.78 2189 CD1 LEU B 403 49.404 75.922 44.456 1.00 35.87 2190 CD2 LEU B 403 49.727 76.744 42.132 1.00 31.42 2191 C LEU B 403 45.910 77.548 44.001 1.00 33.39 2192 O LEU B 403 45.595 78.279 43.060 1.00 30.14 2193 N PRO B 404 45.967 77.996 45.265 1.00 34.13 2194 CD PRO B 404 46.187 77.209 46.495 1.00 34.29 2195 CA PRO B 404 45.701 79.397 45.587 1.00 34.91 2196 CB PRO B 404 45.823 79.439 47.108 1.00 33.92 2197 CG PRO B 404 45.479 78.046 47.526 1.00 33.77 2198 C PRO B 404 46.827 80.173 44.909 1.00 36.43 2199 O PRO B 404 47.990 79.776 44.960 1.00 30.87 2200 N VAL B 405 46.480 81.274 44.265 1.00 37.52 2201 CA VAL B 405 47.471 82.068 43.569 1.00 41.37 2202 CB VAL B 405 47.138 82.078 42.047 1.00 44.39 2203 CG1 VAL B 405 47.034 83.500 41.513 1.00 47.81 2204 CG2 VAL B 405 48.180 81.288 41.301 1.00 43.63 2205 C VAL B 405 47.544 83.492 44.120 1.00 42.93 2206 O VAL B 405 46.553 84.042 44.589 1.00 42.10 2207 N GLY B 406 48.732 84.082 44.081 1.00 45.32 2208 CA GLY B 406 48.869 85.446 44.553 1.00 46.40 2209 C GLY B 406 48.208 86.373 43.548 1.00 46.70 2210 O GLY B 406 48.345 86.179 42.334 1.00 41.89 2211 N THR B 407 47.486 87.373 44.052 1.00 46.37 2212 CA THR B 407 46.791 88.341 43.208 1.00 49.05 2213 CB THR B 407 45.983 89.348 44.062 1.00 51.01 2214 OG1 THR B 407 44.900 88.671 44.709 1.00 55.76 2215 CG2 THR B 407 45.423 90.453 43.195 1.00 54.66 2216 C THR B 407 47.746 89.132 42.325 1.00 49.24 2217 O THR B 407 47.597 89.154 41.105 1.00 48.91 2218 N ALA B 408 48.726 89.777 42.953 1.00 49.71 2219 CA ALA B 408 49.693 90.592 42.240 1.00 50.13 2220 CB ALA B 408 50.562 91.367 43.224 1.00 53.74 2221 C ALA B 408 50.569 89.777 41.312 1.00 51.25 2222 O ALA B 408 50.852 90.207 40.191 1.00 50.28 2223 N ASP B 409 51.000 88.605 41.770 1.00 50.74 2224 CA ASP B 409 51.852 87.748 40.948 1.00 52.13 2225 CB ASP B 409 52.265 86.498 41.730 1.00 58.27 2226 CG ASP B 409 53.065 86.830 42.977 1.00 69.38 2227 OD1 ASP B 409 54.121 87.495 42.848 1.00 75.94 2228 OD2 ASP B 409 52.641 86.431 44.084 1.00 72.00 2229 C ASP B 409 51.151 87.341 39.655 1.00 49.96 2230 O ASP B 409 51.769 87.283 38.588 1.00 49.48 2231 N TRP B 410 49.858 87.058 39.755 1.00 46.74 2232 CA TRP B 410 49.106 86.669 38.583 1.00 44.75 2233 CB TRP B 410 47.732 86.113 38.957 1.00 39.75 2234 CG TRP B 410 46.999 85.687 37.738 1.00 37.35 2235 CD2 TRP B 410 47.191 84.469 37.017 1.00 31.03 2236 CE2 TRP B 410 46.412 84.551 35.846 1.00 29.68 2237 CE3 TRP B 410 47.963 83.314 37.243 1.00 32.46 2238 CD1 TRP B 410 46.119 86.434 37.001 1.00 32.61 2239 NE1 TRP B 410 45.767 85.758 35.868 1.00 33.45 2240 CZ2 TRP B 410 46.370 83.522 34.900 1.00 29.11 2241 CZ3 TRP B 410 47.920 82.290 36.302 1.00 34.12 2242 CH2 TRP B 410 47.128 82.405 35.142 1.00 35.80 2243 C TRP B 410 48.934 87.857 37.649 1.00 43.08 2244 O TRP B 410 49.137 87.733 36.445 1.00 38.95 2245 N ILE B 411 48.563 89.007 38.206 1.00 46.39 2246 CA ILE B 411 48.372 90.211 37.404 1.00 51.22 2247 CB ILE B 411 47.848 91.382 38.259 1.00 53.02 2248 CG2 ILE B 411 47.705 92.628 37.401 1.00 55.27 2249 CG1 ILE B 411 46.488 91.010 38.860 1.00 56.63 2250 CD1 ILE B 411 45.858 92.102 39.733 1.00 61.16 2251 C ILE B 411 49.669 90.632 36.729 1.00 52.33 2252 O ILE B 411 49.645 91.196 35.638 1.00 53.32 2253 N GLU B 412 50.800 90.333 37.369 1.00 54.18 2254 CA GLU B 412 52.099 90.693 36.821 1.00 53.56 2255 CB GLU B 412 53.110 90.908 37.942 1.00 58.95 2256 CG GLU B 412 53.034 92.302 38.528 1.00 73.61 2257 CD GLU B 412 54.062 92.542 39.612 1.00 83.01 2258 OE1 GLU B 412 55.244 92.185 39.411 1.00 89.18 2259 OE2 GLU B 412 53.691 93.102 40.665 1.00 89.24 2260 C GLU B 412 52.665 89.726 35.793 1.00 51.42 2261 O GLU B 412 53.725 89.985 35.227 1.00 50.68 2262 N GLY B 413 51.967 88.617 35.551 1.00 48.27 2263 CA GLY B 413 52.428 87.671 34.551 1.00 46.15 2264 C GLY B 413 53.111 86.377 34.967 1.00 44.58 2265 O GLY B 413 53.637 85.675 34.106 1.00 42.91 2266 N GLU B 414 53.118 86.044 36.256 1.00 44.06 2267 CA GLU B 414 53.749 84.799 36.685 1.00 42.21 2268 CB GLU B 414 53.467 84.523 38.172 1.00 42.27 2269 CG GLU B 414 53.963 83.159 38.698 1.00 44.30 2270 CD GLU B 414 55.487 83.036 38.739 1.00 52.18 2271 OE1 GLU B 414 56.083 82.562 37.745 1.00 51.39 2272 OE2 GLU B 414 56.090 83.425 39.764 1.00 49.53 2273 C GLU B 414 53.147 83.690 35.839 1.00 41.40 2274 O GLU B 414 51.995 83.781 35.413 1.00 38.41 2275 N THR B 415 53.936 82.656 35.573 1.00 41.90 2276 CA THR B 415 53.454 81.522 34.806 1.00 43.26 2277 CB THR B 415 54.281 81.341 33.506 1.00 46.09 2278 OG1 THR B 415 54.155 79.996 33.032 1.00 50.78 2279 CG2 THR B 415 55.716 81.690 33.734 1.00 56.55 2280 C THR B 415 53.499 80.270 35.690 1.00 41.87 2281 O THR B 415 54.533 79.963 36.285 1.00 43.61 2282 N TYR B 416 52.371 79.571 35.806 1.00 39.27 2283 CA TYR B 416 52.309 78.378 36.650 1.00 37.37 2284 CB TYR B 416 51.102 78.428 37.581 1.00 33.61 2285 CG TYR B 416 51.064 79.633 38.478 1.00 27.57 2286 CD1 TYR B 416 50.753 80.894 37.974 1.00 26.31 2287 CE1 TYR B 416 50.752 82.009 38.800 1.00 35.08 2288 CD2 TYR B 416 51.371 79.516 39.825 1.00 28.68 2289 CE2 TYR B 416 51.379 80.615 40.651 1.00 30.56 2290 CZ TYR B 416 51.070 81.857 40.140 1.00 35.62 2291 OH TYR B 416 51.088 82.944 40.984 1.00 44.94 2292 C TYR B 416 52.256 77.106 35.833 1.00 38.31 2293 O TYR B 416 51.744 77.092 34.709 1.00 37.29 2294 N GLN B 417 52.781 76.031 36.416 1.00 39.74 2295 CA GLN B 417 52.823 74.751 35.736 1.00 40.75 2296 CB GLN B 417 54.254 74.457 35.264 1.00 41.60 2297 CG GLN B 417 54.353 73.240 34.349 1.00 53.57 2298 CD GLN B 417 55.762 72.997 33.829 1.00 65.04 2299 OE1 GLN B 417 56.481 72.124 34.325 1.00 69.74 2300 NE2 GLN B 417 56.165 73.777 32.831 1.00 66.91 2301 C GLN B 417 52.320 73.578 36.565 1.00 39.48 2302 O GLN B 417 52.619 73.451 37.754 1.00 40.03 2303 N CYS B 418 51.557 72.718 35.912 1.00 39.47 2304 CA CYS B 418 51.032 71.525 36.541 1.00 41.39 2305 C CYS B 418 51.732 70.354 35.868 1.00 41.00 2306 O CYS B 418 51.661 70.205 34.648 1.00 41.94 2307 CB CYS B 418 49.513 71.413 36.319 1.00 39.12 2308 SG CYS B 418 48.782 69.912 37.050 1.00 53.87 2309 N ALA B 419 52.429 69.541 36.654 1.00 42.75 2310 CA ALA B 419 53.102 68.362 36.118 1.00 45.21 2311 CB ALA B 419 54.527 68.243 36.688 1.00 45.00 2312 C ALA B 419 52.265 67.138 36.498 1.00 46.28 2313 O ALA B 419 52.172 66.774 37.671 1.00 44.60 2314 N VAL B 420 51.639 66.512 35.508 1.00 49.65 2315 CA VAL B 420 50.811 65.348 35.778 1.00 54.91 2316 CB VAL B 420 49.584 65.305 34.855 1.00 52.57 2317 CG1 VAL B 420 48.742 64.085 35.189 1.00 54.41 2318 CG2 VAL B 420 48.756 66.568 35.017 1.00 52.89 2319 C VAL B 420 51.572 64.036 35.623 1.00 59.75 2320 O VAL B 420 52.083 63.723 34.544 1.00 56.32 2321 N THR B 421 51.640 63.275 36.713 1.00 65.72 2322 CA THR B 421 52.322 61.985 36.717 1.00 72.95 2323 CB THR B 421 53.303 61.867 37.903 1.00 73.73 2324 OG1 THR B 421 54.294 62.898 37.818 1.00 78.26 2325 CG2 THR B 421 53.995 60.518 37.883 1.00 74.84 2326 C THR B 421 51.302 60.859 36.831 1.00 76.77 2327 O THR B 421 50.937 60.459 37.936 1.00 76.76 2328 N ALA B 422 50.843 60.352 35.690 1.00 81.68 2329 CA ALA B 422 49.862 59.270 35.673 1.00 86.81 2330 CB ALA B 422 49.134 59.242 34.332 1.00 86.67 2331 C ALA B 422 50.540 57.930 35.922 1.00 90.55 2332 O ALA B 422 51.724 57.757 35.623 1.00 91.00 2333 N PRO B 423 49.793 56.959 36.475 1.00 93.77 2334 CD PRO B 423 48.340 56.985 36.715 1.00 94.85 2335 CA PRO B 423 50.343 55.630 36.759 1.00 95.83 2336 CB PRO B 423 49.141 54.869 37.309 1.00 96.70 2337 CG PRO B 423 47.981 55.526 36.613 1.00 97.10 2338 C PRO B 423 50.926 54.988 35.504 1.00 97.16 2339 O PRO B 423 52.128 54.750 35.426 1.00 97.34 2340 N ALA B 424 50.076 54.707 34.522 1.00 98.50 2341 CA ALA B 424 50.537 54.114 33.271 1.00 99.73 2342 CB ALA B 424 49.348 53.605 32.474 1.00 99.11 2343 C ALA B 424 51.282 55.188 32.475 1.00 100.69 2344 O ALA B 424 51.875 56.097 33.054 1.00 101.64 2345 N LEU B 425 51.245 55.079 31.150 1.00 100.65 2346 CA LEU B 425 51.895 56.050 30.272 1.00 99.91 2347 CB LEU B 425 51.228 57.418 30.429 1.00 100.27 2348 CG LEU B 425 49.767 57.474 29.975 1.00 102.88 2349 CD1 LEU B 425 49.214 58.865 30.211 1.00 102.68 2350 CD2 LEU B 425 49.668 57.102 28.497 1.00 105.00 2351 C LEU B 425 53.400 56.173 30.514 1.00 98.82 2352 O LEU B 425 53.924 55.615 31.471 1.00 98.87 2353 N PRO B 426 54.115 56.888 29.625 1.00 97.69 2354 CD PRO B 426 53.661 57.182 28.251 1.00 98.02 2355 CA PRO B 426 55.566 57.087 29.739 1.00 95.83 2356 CB PRO B 426 56.030 56.927 28.303 1.00 96.48 2357 CG PRO B 426 54.941 57.635 27.555 1.00 96.97 2358 C PRO B 426 55.949 58.455 30.309 1.00 94.21 2359 O PRO B 426 56.240 58.594 31.498 1.00 94.03 2360 N ARG B 427 55.963 59.460 29.439 1.00 92.33 2361 CA ARG B 427 56.303 60.822 29.831 1.00 90.72 2362 CB ARG B 427 56.583 61.672 28.590 1.00 92.36 2363 CG ARG B 427 57.784 61.251 27.758 1.00 96.36 2364 CD ARG B 427 59.015 62.075 28.102 1.00 99.46 2365 NE ARG B 427 59.822 62.353 26.916 1.00 101.30 2366 CZ ARG B 427 59.397 63.060 25.872 1.00 102.28 2367 NH1 ARG B 427 58.170 63.563 25.864 1.00 102.89 2368 NH2 ARG B 427 60.200 63.266 24.836 1.00 102.96 2369 C AEG B 427 55.142 61.448 30.595 1.00 88.67 2370 O ARG B 427 53.986 61.308 30.198 1.00 88.90 2371 N ALA B 428 55.447 62.138 31.687 1.00 85.79 2372 CA ALA B 428 54.412 62.793 32.469 1.00 82.45 2373 CB ALA B 428 54.985 63.290 33.789 1.00 82.49 2374 C ALA B 428 53.893 63.963 31.644 1.00 79.74 2375 O ALA B 428 54.645 64.568 30.879 1.00 79.87 2376 N LEU B 429 52.606 64.270 31.785 1.00 76.91 2377 CA LEU B 429 51.996 65.377 31.051 1.00 72.60 2378 CB LEU B 429 50.475 65.195 30.974 1.00 73.30 2379 CG LEU B 429 49.915 63.916 30.343 1.00 75.14 2380 CD1 LEU B 429 48.403 63.894 30.500 1.00 70.88 2381 CD2 LEU B 429 50.304 63.844 28.873 1.00 79.00 2382 C LEU B 429 52.310 66.679 31.777 1.00 69.58 2383 O LEU B 429 52.391 66.706 33.006 1.00 67.68 2384 N MET B 430 52.484 67.755 31.015 1.00 66.58 2385 CA MET B 430 52.785 69.057 31.596 1.00 63.72 2386 CB MET B 430 54.260 69.397 31.396 1.00 66.69 2387 CG MET B 430 55.205 68.363 31.975 1.00 76.81 2388 SD MET B 430 56.932 68.836 31.755 1.00 89.36 2389 CE MET B 430 57.129 68.610 29.990 1.00 87.45 2390 C MET B 430 51.926 70.150 30.981 1.00 59.15 2391 O MET B 430 51.778 70.229 29.760 1.00 59.09 2392 N ARG B 431 51.355 70.993 31.833 1.00 55.24 2393 CA AEG B 431 50.509 72.077 31.354 1.00 51.07 2394 CB ARG B 431 49.036 71.737 31.584 1.00 51.17 2395 CG ARG B 431 48.661 70.309 31.203 1.00 55.59 2396 CD ARG B 431 47.441 70.280 30.295 1.00 67.55 2397 NE ARG B 431 47.784 70.453 28.884 1.00 74.62 2398 CZ ARG B 431 48.220 69.472 28.099 1.00 76.90 2399 NH1 ARG B 431 48.364 68.247 28.586 1.00 77.02 2400 NH2 ARG B 431 48.513 69.712 26.826 1.00 79.64 2401 C ARG B 431 50.868 73.356 32.087 1.00 47.90 2402 O ARG B 431 51.214 73.323 33.268 1.00 46.26 2403 N SER B 432 50.788 74.480 31.385 1.00 45.54 2404 CA SER B 432 51.105 75.768 31.988 1.00 45.94 2405 CB SER B 432 52.484 76.244 31.516 1.00 47.12 2406 OC SER B 432 52.560 76.269 30.106 1.00 50.92 2407 C SER B 432 50.063 76.836 31.688 1.00 43.27 2408 O SER B 432 49.328 76.738 30.709 1.00 42.70 2409 N THR B 433 50.012 77.864 32.531 1.00 40.97 2410 CA THR B 433 49.048 78.937 32.342 1.00 38.90 2411 CB THR B 433 47.725 78.633 33.073 1.00 39.50 2412 OG1 THR B 433 46.792 79.689 32.820 1.00 38.91 2413 CG2 THR B 433 47.954 78.507 34.584 1.00 36.51 2414 C THR B 433 49.583 80.271 32.838 1.00 39.62 2415 O THR B 433 50.412 80.317 33.744 1.00 39.87 2416 N THR B 434 49.105 81.351 32.224 1.00 39.10 2417 CA THR B 434 49.499 82.711 32.569 1.00 39.67 2418 CB THR B 434 50.788 83.120 31.818 1.00 43.40 2419 OG1 THR B 434 50.496 83.293 30.425 1.00 53.59 2420 CG2 THR B 434 51.830 82.041 31.929 1.00 52.29 2421 C THR B 434 48.380 83.661 32.131 1.00 38.41 2422 O THR B 434 47.490 83.275 31.374 1.00 38.84 2423 N ALA B 435 48.421 84.899 32.594 1.00 37.73 2424 CA ALA B 435 47.410 85.853 32.189 1.00 44.38 2425 CB ALA B 435 47.632 87.174 32.887 1.00 40.72 2426 C ALA B 435 47.567 86.023 30.679 1.00 47.78 2427 O ALA B 435 48.681 85.989 30.163 1.00 46.98 2428 N TNR B 436 46.454 86.187 29.971 1.00 52.31 2429 CA THR B 436 46.506 86.383 28.526 1.00 55.83 2430 CB THR B 436 45.131 86.108 27.860 1.00 59.83 2431 OG1 THR B 436 44.784 84.727 28.028 1.00 62.64 2432 CG2 THR B 436 45.175 86.441 26.368 1.00 60.56 2433 C THR B 436 46.893 87.834 28.260 1.00 56.91 2434 O THR B 436 46.358 88.748 28.888 1.00 55.51 2435 N SER B 437 47.841 88.043 27.352 1.00 58.87 2436 CA SER B 437 48.256 89.398 27.005 1.00 61.80 2437 CB SER B 437 49.746 89.445 26.626 1.00 63.69 2438 OG SER B 437 50.029 88.616 25.511 1.00 67.24 2439 C SER B 437 47.397 89.847 25.828 1.00 61.35 2440 O SER B 437 46.489 89.123 25.410 1.00 61.92 2441 N GLY B 438 47.670 91.033 25.297 1.00 60.43 2442 CA GLY B 438 46.881 91.513 24.177 1.00 59.27 2443 C GLY B 438 45.909 92.601 24.590 1.00 58.25 2444 O GLY B 438 45.753 92.861 25.779 1.00 58.13 2445 N PRO B 439 45.237 93.253 23.628 1.00 58.84 2446 CD PRO B 439 45.385 93.045 22.177 1.00 60.09 2447 CA PRO B 439 44.277 94.325 23.897 1.00 57.04 2448 CB PRO B 439 43.768 94.692 22.503 1.00 57.59 2449 CG PRO B 439 44.933 94.376 21.628 1.00 59.40 2450 C PRO B 439 43.147 93.909 24.828 1.00 54.66 2451 O PRO B 439 42.824 92.723 24.945 1.00 56.08 2452 N ARG B 440 42.548 94.897 25.482 1.00 51.95 2453 CA ARG B 440 41.451 94.658 26.405 1.00 49.50 2454 CB ARG B 440 41.829 95.129 27.817 1.00 51.89 2455 CG ARG B 440 43.200 94.679 28.309 1.00 59.84 2456 CD ARG B 440 43.266 93.188 28.635 1.00 66.22 2457 NE ARG B 440 44.657 92.755 28.787 1.00 74.61 2458 CZ ARG B 440 45.045 91.553 29.204 1.00 76.10 2459 NH1 ARG B 440 44.156 90.633 29.527 1.00 77.20 2460 NH2 ARG B 440 46.338 91.272 29.295 1.00 84.96 2461 C ARG B 440 40.249 95.455 25.910 1.00 46.80 2462 O ARG B 440 40.406 96.542 25.354 1.00 46.09 2463 N ALA B 441 39.053 94.904 26.099 1.00 42.67 2464 CA ALA B 441 37.821 95.576 25.698 1.00 39.13 2465 CB ALA B 441 37.458 95.216 24.263 1.00 32.25 2466 C ALA B 441 36.712 95.142 26.646 1.00 39.00 2467 O ALA B 441 36.555 93.961 26.925 1.00 38.16 2468 N ALA B 442 35.949 96.118 27.136 1.00 37.20 2469 CA ALA B 442 34.861 95.864 28.063 1.00 37.26 2470 CB ALA B 442 34.312 97.187 28.574 1.00 37.47 2471 C ALA B 442 33.718 95.032 27.483 1.00 39.85 2472 O ALA B 442 33.510 94.988 26.275 1.00 41.57 2473 N PRO B 443 32.960 94.354 28.357 1.00 39.83 2474 CD PRO B 443 33.303 94.122 29.766 1.00 40.96 2475 CA PRO B 443 31.825 93.520 27.969 1.00 38.29 2476 CB PRO B 443 31.678 92.542 29.144 1.00 36.98 2477 CG PRO B 443 32.925 92.693 29.932 1.00 36.14 2478 C PRO B 443 30.563 94.380 27.828 1.00 40.19 2479 O PRO B 443 30.406 95.396 28.512 1.00 40.51 2480 N ALA B 444 29.673 93.964 26.937 1.00 39.07 2481 CA ALA B 444 28.412 94.658 26.724 1.00 36.58 2482 CB ALA B 444 28.228 94.995 25.240 1.00 40.22 2483 C ALA B 444 27.373 93.638 27.181 1.00 34.33 2484 O ALA B 444 27.358 92.491 26.702 1.00 30.65 2485 N VAL B 445 26.519 94.057 28.109 1.00 28.37 2486 CA VAL B 445 25.520 93.172 28.664 1.00 26.39 2487 CB VAL B 445 25.652 93.152 30.198 1.00 26.69 2488 CG1 VAL B 445 24.620 92.205 30.790 1.00 23.97 2489 CG2 VAL B 445 27.076 92.747 30.586 1.00 22.56 2490 C VAL B 445 24.068 93.497 28.291 1.00 27.26 2491 O VAL B 445 23.646 94.644 28.367 1.00 24.12 2492 N TYR B 446 23.319 92.473 27.893 1.00 23.45 2493 CA TYR B 446 21.919 92.645 27.541 1.00 25.54 2494 CB TYR B 446 21.722 92.732 26.015 1.00 24.97 2495 CG TYR B 446 20.264 92.896 25.660 1.00 24.95 2496 CD1 TYR B 446 19.517 93.961 26.182 1.00 37.39 2497 CE1 TYR B 446 18.146 94.094 25.907 1.00 34.09 2498 CD2 TYR B 446 19.613 91.973 24.851 1.00 28.20 2499 CE2 TYR B 446 18.245 92.092 24.567 1.00 31.02 2500 CZ TYR B 446 17.519 93.160 25.102 1.00 34.30 2501 OH TYR B 446 16.174 93.294 24.846 1.00 35.42 2502 C TYR B 446 21.130 91.465 28.088 1.00 23.87 2503 O TYR B 446 21.321 90.325 27.663 1.00 28.38 2504 N ALA B 447 20.254 91.742 29.042 1.00 26.40 2505 CA ALA B 447 19.445 90.707 29.671 1.00 27.30 2506 CB ALA B 447 19.535 90.834 31.195 1.00 24.55 2507 C ALA B 447 18.002 90.840 29.202 1.00 30.87 2508 O ALA B 447 17.515 91.945 28.979 1.00 32.42 2509 N PHE B 448 17.310 89.720 29.045 1.00 31.33 2510 CA PHE B 448 15.939 89.799 28.582 1.00 34.25 2511 CB PHE B 448 15.938 89.984 27.060 1.00 40.48 2512 CG PHE B 448 16.497 88.805 26.314 1.00 39.26 2513 CD1 PHE B 448 15.663 87.763 25.923 1.00 39.27 2514 CD2 PHE B 448 17.862 88.704 26.059 1.00 36.97 2515 CE1 PHE B 448 16.180 86.633 25.286 1.00 43.41 2516 CE2 PHE B 448 18.389 87.578 25.422 1.00 36.78 2517 CZ PHE B 448 17.546 86.541 25.036 1.00 37.14 2518 C PHE B 448 15.113 88.579 28.952 1.00 34.75 2519 O PHE B 448 15.646 87.554 29.369 1.00 34.97 2520 N ALA B 449 13.801 88.708 28.798 1.00 37.02 2521 CA ALA B 449 12.877 87.623 29.079 1.00 38.65 2522 CB ALA B 449 11.731 88.122 29.898 1.00 32.34 2523 C ALA B 449 12.350 87.050 27.767 1.00 42.92 2524 O ALA B 449 12.165 87.774 26.794 1.00 42.07 2525 N THR B 450 12.111 85.743 27.759 1.00 47.71 2526 CA THR B 450 11.586 85.048 26.597 1.00 52.16 2527 CB THR B 450 12.040 83.577 26.599 1.00 53.90 2528 OG1 THR B 450 13.468 83.522 26.685 1.00 61.82 2529 CG2 THR B 450 11.594 82.877 25.327 1.00 62.58 2530 C THR B 450 10.053 85.097 26.607 1.00 54.69 2531 O THR B 450 9.421 84.983 27.659 1.00 51.28 2532 N PRO B 451 9.439 85.280 25.431 1.00 57.24 2533 CD PRO B 451 10.061 85.618 24.137 1.00 60.66 2534 CA PRO B 451 7.977 85.339 25.338 1.00 61.04 2535 CB PRO B 451 7.736 85.571 23.846 1.00 61.38 2536 CG PRO B 451 8.946 86.360 23.433 1.00 63.63 2537 C PRO B 451 7.301 84.063 25.847 1.00 63.11 2538 O PRO B 451 7.682 82.949 25.484 1.00 61.66 2539 N GLU B 452 6.303 84.230 26.706 1.00 66.04 2540 CA GLU B 452 5.575 83.083 27.237 1.00 69.40 2541 CB GLU B 452 5.800 82.954 28.753 1.00 67.34 2542 CG GLU B 452 5.911 81.505 29.277 1.00 60.86 2543 CD GLU B 452 7.225 80.815 28.876 1.00 59.08 2544 OE1 GLU B 452 8.255 81.510 28.775 1.00 62.62 2545 OE2 GLU B 452 7.249 79.578 28.676 1.00 45.82 2546 C GLU B 452 4.090 83.278 26.930 1.00 71.98 2547 O GLU B 452 3.360 83.895 27.705 1.00 70.35 2548 N ALA B 453 3.659 82.758 25.783 1.00 75.33 2549 CA ALA B 453 2.266 82.867 25.347 1.00 78.80 2550 CB ALA B 453 2.075 82.118 24.029 1.00 80.74 2551 C ALA B 453 1.282 82.340 26.394 1.00 80.53 2552 O ALA B 453 1.599 81.433 27.167 1.00 82.95 2553 N LYS B 459 8.685 75.798 30.647 1.00 51.87 2554 CA LYS B 459 9.250 76.647 31.693 1.00 52.84 2555 CB LYS B 459 10.479 75.987 32.317 1.00 55.20 2556 CG LYS B 459 10.171 74.721 33.089 1.00 63.98 2557 CD LYS B 459 11.271 74.401 34.088 1.00 72.67 2558 CE LYS B 459 11.366 75.484 35.157 1.00 77.63 2559 NZ LYS B 459 12.302 75.122 36.259 1.00 83.78 2560 C LYS B 459 9.638 78.033 31.195 1.00 50.86 2561 O LYS B 459 10.211 78.174 30.118 1.00 49.65 2562 N ARG B 460 9.332 79.045 32.001 1.00 48.30 2563 CA ARG B 460 9.640 80.433 31.674 1.00 47.61 2564 CB ARG B 460 8.865 81.350 32.620 1.00 51.65 2565 CG ARG B 460 7.371 81.029 32.591 1.00 59.85 2566 CD ARG B 460 6.570 81.784 33.635 1.00 65.41 2567 NE ARG B 460 5.158 81.400 33.603 1.00 70.36 2568 CZ ARG B 460 4.702 80.174 33.848 1.00 73.06 2569 NH1 ARG B 460 5.540 79.188 34.150 1.00 75.61 2570 NH2 ARG B 460 3.401 79.929 33.791 1.00 76.52 2571 C ARG B 460 11.154 80.664 31.759 1.00 44.39 2572 O ARG B 460 11.839 80.058 32.589 1.00 41.11 2573 N THR B 461 11.672 81.540 30.905 1.00 40.18 2574 CA THR B 461 13.111 81.768 30.850 1.00 40.02 2575 CB THR B 461 13.733 80.985 29.659 1.00 41.84 2576 OG1 THR B 461 13.383 79.601 29.750 1.00 52.98 2577 CG2 THR B 461 15.238 81.102 29.666 1.00 48.91 2578 C THR B 461 13.574 83.207 30.699 1.00 37.19 2579 O THR B 461 12.959 84.009 29.982 1.00 37.94 2580 N LEU B 462 14.681 83.512 31.375 1.00 33.00 2581 CA LEU B 462 15.335 84.809 31.289 1.00 29.46 2582 CB LEU B 462 15.550 85.434 32.667 1.00 30.35 2583 CG LEU B 462 14.282 85.678 33.498 1.00 33.09 2584 CD1 LEU B 462 14.639 86.412 34.785 1.00 32.32 2585 CD2 LEU B 462 13.293 86.499 32.699 1.00 25.52 2586 C LEU B 462 16.672 84.439 30.662 1.00 29.44 2587 O LEU B 462 17.184 83.339 30.894 1.00 24.62 2588 N ALA B 463 17.237 85.343 29.868 1.00 27.23 2589 CA ALA B 463 18.486 85.050 29.192 1.00 27.78 2590 CB ALA B 463 18.199 84.488 27.790 1.00 26.61 2591 C ALA B 463 19.332 86.301 29.104 1.00 28.37 2592 O ALA B 463 18.824 87.415 29.233 1.00 29.09 2593 N CYS B 464 20.623 86.115 28.870 1.00 22.40 2594 CA CYS B 464 21.534 87.246 28.821 1.00 26.72 2595 C CYS B 464 22.622 87.038 27.786 1.00 24.16 2596 O CYS B 464 23.199 85.952 27.691 1.00 23.01 2597 CB CYS B 464 22.172 87.410 30.200 1.00 24.58 2598 SG CYS B 464 23.327 88.794 30.423 1.00 40.31 2599 N LEU B 465 22.908 88.096 27.032 1.00 22.68 2600 CA LEU B 465 23.950 88.052 26.013 1.00 24.31 2601 CB LEU B 465 23.390 88.473 24.640 1.00 26.81 2602 CG LEU B 465 24.419 88.841 23.554 1.00 21.10 2603 CD1 LEU B 465 25.310 87.659 23.251 1.00 21.73 2604 CD2 LEU B 465 23.700 89.262 22.293 1.00 30.90 2605 C LEU B 465 25.043 89.013 26.453 1.00 23.79 2606 O LEU B 465 24.770 90.183 26.741 1.00 22.87 2607 N ILE B 466 26.276 88.521 26.510 1.00 23.16 2608 CA ILE B 466 27.402 89.349 26.926 1.00 23.50 2609 CB ILE B 466 28.018 88.838 28.251 1.00 23.66 2610 CG2 ILE B 466 29.140 89.800 28.705 1.00 29.47 2611 CG1 ILE B 466 26.913 88.739 29.320 1.00 19.89 2612 CG1 ILE B 466 27.398 88.229 30.650 1.00 36.91 2613 C ILE B 466 28.388 89.274 25.784 1.00 22.24 2614 O ILE B 466 28.811 88.189 25.385 1.00 24.74 2615 N GLN B 467 28.789 90.433 25.270 1.00 23.91 2616 CA GLN B 467 29.642 90.418 24.095 1.00 31.01 2617 CB GLN B 467 28.747 90.376 22.846 1.00 30.11 2618 CG GLN B 467 27.869 91.607 22.654 1.00 26.37 2619 CD GLN B 467 26.920 91.486 21.464 1.00 29.83 2620 OE1 GLN B 467 27.136 90.710 20.521 1.00 28.59 2621 NE2 GLN B 467 25.869 92.282 21.495 1.00 31.49 2622 C GLN B 467 30.641 91.546 23.952 1.00 33.72 2623 O GLN B 467 30.691 92.469 24.768 1.00 31.53 2624 N ASN B 468 31.442 91.421 22.895 1.00 38.27 2625 CA ASN B 468 32.465 92.385 22.526 1.00 41.08 2626 CB ASN B 468 31.839 93.744 22.245 1.00 43.70 2627 CG ASN B 468 30.665 93.651 21.303 1.00 50.48 2628 OD1 ASN B 468 30.722 92.959 20.281 1.00 59.45 2629 ND2 ASN B 468 29.594 94.357 21.628 1.00 56.28 2630 C ASN B 468 33.560 92.548 23.554 1.00 41.04 2631 O ASN B 468 34.155 93.614 23.660 1.00 38.53 2632 N PHE B 469 33.843 91.499 24.309 1.00 38.66 2633 CA PHE B 469 34.894 91.604 25.303 1.00 38.07 2634 CB PHE B 469 34.360 91.181 26.673 1.00 29.35 2635 CG PHE B 469 34.064 89.712 26.791 1.00 28.48 2636 CG1 PHE B 469 35.059 88.815 27.113 1.00 23.56 2637 CD2 PHE B 469 32.777 89.231 26.579 1.00 24.16 2638 CE1 PHE B 469 34.784 87.463 27.228 1.00 27.41 2639 CE2 PHE B 469 32.493 87.867 26.691 1.00 32.69 2640 CZ PHE B 469 33.506 86.984 27.017 1.00 24.40 2641 C PHE B 469 36.125 90.785 24.939 1.00 38.11 2642 O PHE B 469 36.026 89.752 24.287 1.00 39.11 2643 N MET B 470 37.287 91.267 25.359 1.00 40.05 2644 CA MET B 470 38.569 90.599 25.130 1.00 41.39 2645 CB MET B 470 39.183 90.982 23.779 1.00 46.13 2646 CG MET B 470 39.557 92.441 23.570 1.00 60.40 2647 SD MET B 470 39.966 92.737 21.820 1.00 65.64 2648 CE MET B 470 41.659 92.059 21.727 1.00 71.36 2649 C MET B 470 39.417 91.095 26.280 1.00 38.04 2650 O MET B 470 39.376 92.273 26.618 1.00 36.87 2651 N PRO B 471 40.184 90.201 26.925 1.00 37.84 2652 CD PRO B 471 40.913 90.654 28.117 1.00 38.40 2653 CA PRO B 471 40.360 88.747 26.742 1.00 37.04 2654 CB PRO B 471 41.485 88.400 27.732 1.00 38.82 2655 CG PRO B 471 42.076 89.748 28.096 1.00 40.26 2656 C PRO B 471 39.092 87.915 26.996 1.00 35.06 2657 O PRO B 471 38.076 88.443 27.432 1.00 33.27 2658 N GLU B 472 39.180 86.611 26.760 1.00 35.63 2659 CA GLU B 472 38.033 85.705 26.898 1.00 38.83 2660 CB GLU B 472 38.292 84.431 26.109 1.00 43.92 2661 CG GLU B 472 39.299 83.516 26.792 1.00 54.98 2662 CD GLU B 472 39.657 82.288 25.963 1.00 65.38 2663 OE1 GLU B 472 39.172 82.169 24.821 1.00 73.96 2664 OE2 GLU B 472 40.433 81.442 26.450 1.00 71.17 2665 C GLU B 472 37.568 85.292 28.294 1.00 36.65 2666 O GLU B 472 36.453 84.801 28.451 1.00 32.41 2667 N ASP B 473 38.402 85.482 29.311 1.00 35.48 2668 CA ASP B 473 38.004 85.092 30.668 1.00 34.00 2669 CB ASP B 473 39.225 85.066 31.594 1.00 39.24 2670 CG ASP B 473 40.239 83.993 31.193 1.00 48.86 2671 OD1 ASP B 473 39.800 82.876 30.817 1.00 42.86 2672 OD2 ASP B 473 41.461 84.270 31.265 1.00 46.87 2673 C ASP B 473 36.917 85.993 31.256 1.00 34.33 2674 O ASP B 473 37.057 87.220 31.315 1.00 34.18 2675 N TLE B 474 35.824 85.384 31.691 1.00 27.93 2676 CA ILE B 474 34.738 86.165 32.254 1.00 28.40 2677 CB ILE B 474 33.848 86.726 31.129 1.00 25.16 2678 CG2 ILE B 474 33.036 85.602 30.489 1.00 26.53 2679 CG1 ILE B 474 32.935 87.828 31.664 1.00 21.56 2680 CD1 ILE B 474 32.219 88.591 30.507 1.00 23.93 2681 C ILE B 474 33.890 85.326 33.190 1.00 26.83 2682 O ILE B 474 33.773 84.127 33.014 1.00 25.94 2683 N SER B 475 33.325 85.975 34.202 1.00 24.54 2684 CA SER B 475 32.446 85.336 35.167 1.00 23.71 2685 CB SER B 475 32.932 85.586 36.590 1.00 22.00 2686 OG SER B 475 34.221 85.045 36.759 1.00 30.00 2687 C SER B 475 31.071 85.967 34.983 1.00 24.55 2688 O SER B 475 30.931 87.190 34.965 1.00 23.24 2689 N VAL B 476 30.058 85.124 34.847 1.00 24.48 2690 CA VAL B 476 28.692 85.562 34.654 1.00 26.25 2691 CB VAL B 476 28.097 84.928 33.379 1.00 24.14 2692 CG1 VAL B 476 26.635 85.340 33.227 1.00 23.36 2693 CG2 VAL B 476 28.907 85.357 32.163 1.00 28.16 2694 C VAL B 476 27.877 85.111 35.847 1.00 28.80 2695 O VAL B 476 28.045 83.993 36.339 1.00 32.13 2696 N GLN B 477 26.993 85.971 36.326 1.00 28.79 2697 CA GLN B 477 26.176 85.589 37.458 1.00 30.02 2698 CB GLN B 477 26.913 85.854 38.774 1.00 31.30 2699 CG GLN B 477 27.360 87.270 38.993 1.00 46.28 2700 CD GLN B 477 28.499 87.368 40.007 1.00 49.95 2701 OE1 GLN B 477 28.842 88.455 40.465 1.00 51.94 2702 NE2 GLN B 477 29.097 86.227 40.349 1.00 51.51 2703 C GLN B 477 24.856 86.313 37.431 1.00 30.41 2704 O GLN B 477 24.757 87.415 36.902 1.00 30.03 2705 N TRP B 478 23.841 85.659 37.976 1.00 29.86 2706 CA TRP B 478 22.505 86.210 38.042 1.00 29.12 2707 CB TRP B 478 21.499 85.165 37.579 1.00 31.11 2708 CG TRP B 478 21.527 84.936 36.112 1.00 36.98 2709 CD2 TRP B 478 20.726 85.605 35.132 1.00 34.77 2710 CE2 TRP B 478 21.092 85.084 33.870 1.00 37.75 2711 CE3 TRP B 478 19.742 86.602 35.194 1.00 31.61 2712 CD1 TRP B 478 22.320 84.060 35.432 1.00 35.86 2713 NE1 TRP B 478 22.065 84.142 34.086 1.00 35.58 2714 CZ2 TRP B 478 20.494 85.521 32.668 1.00 26.96 2715 CZ3 TRP B 478 19.148 87.039 34.005 1.00 35.86 2716 CH2 TRP B 478 19.531 86.497 32.757 1.00 31.66 2717 C TRP B 478 22.175 86.648 39.468 1.00 29.01 2718 O TRP B 478 22.580 86.006 40.439 1.00 24.19 2719 N LEU B 479 21.436 87.742 39.582 1.00 31.15 2720 CA LEU B 479 21.042 88.275 40.880 1.00 36.67 2721 CB LEU B 479 21.837 89.537 41.198 1.00 41.07 2722 CG LEU B 479 23.328 89.584 40.867 1.00 48.71 2723 CD1 LEU B 479 23.889 90.861 41.440 1.00 57.57 2724 CD2 LEU B 479 24.054 88.396 41.455 1.00 56.00 2725 C LEU B 479 19.556 88.624 40.920 1.00 38.99 2726 O LEU B 479 18.965 88.998 39.909 1.00 37.96 2727 N HIS B 480 18.963 88.500 42.096 1.00 42.00 2728 CA HIS B 480 17.561 88.834 42.284 1.00 48.67 2729 CB HIS B 480 16.784 87.648 42.871 1.00 50.22 2730 CG HIS B 480 15.309 87.894 43.014 1.00 53.99 2731 CD2 HIS B 480 14.256 87.041 42.993 1.00 56.80 2732 ND1 HIS B 480 14.779 89.147 43.239 1.00 54.56 2733 CE1 HIS B 480 13.465 89.057 43.348 1.00 60.76 2734 NE2 HIS B 480 13.122 87.789 43.203 1.00 59.92 2735 C HIS B 480 17.625 89.972 43.283 1.00 52.66 2736 O HIS B 480 17.426 89.777 44.482 1.00 51.85 2737 N ASN B 481 17.945 91.161 42.780 1.00 58.88 2738 CA ASN B 481 18.062 92.339 43.628 1.00 63.74 2739 CB ASN B 481 16.763 92.588 44.407 1.00 69.70 2740 CG ASN B 481 15.674 93.211 43.561 1.00 76.04 2741 OD1 ASN B 481 14.513 93.246 43.962 1.00 80.67 2742 ND2 ASN B 481 16.042 93.719 42.392 1.00 82.88 2743 C ASN B 481 19.182 92.134 44.633 1.00 63.93 2744 O ASN B 481 19.008 91.402 45.604 1.00 67.09 2745 N GLU B 482 20.322 92.781 44.399 1.00 62.43 2746 CA GLU B 482 21.477 92.715 45.299 1.00 60.15 2747 CB GLU B 482 21.225 93.623 46.519 1.00 65.85 2748 CG GLU B 482 19.754 94.021 46.707 1.00 78.14 2749 CD GLU B 482 19.282 93.946 48.144 1.00 84.88 2750 OE1 GLU B 482 19.662 92.984 48.846 1.00 90.19 2751 OE2 GLU B 482 18.518 94.841 48.566 1.00 87.19 2752 C GLU B 482 21.949 91.331 45.786 1.00 54.93 2753 O GLU B 482 23.084 91.194 46.247 1.00 57.04 2754 N VAL B 483 21.111 90.305 45.686 1.00 49.03 2755 CA VAL B 483 21.511 88.987 46.163 1.00 45.46 2756 CB VAL B 483 20.450 88.391 47.126 1.00 43.71 2757 CG1 VAL B 483 19.099 88.280 46.427 1.00 50.19 2758 CG2 VAL B 483 20.913 87.033 47.633 1.00 43.76 2759 C VAL B 483 21.758 88.016 45.022 1.00 43.31 2760 O VAL B 483 20.924 87.859 44.137 1.00 41.21 2761 N CLN B 484 22.913 87.362 45.061 1.00 42.10 2762 CA GLN B 484 23.303 86.411 44.036 1.00 41.31 2763 CB CLN B 484 24.822 86.251 44.047 1.00 46.93 2764 CG GLN B 484 25.338 85.180 43.107 1.00 54.66 2765 CD GLN B 484 26.851 85.172 42.999 1.00 61.50 2766 OE1 GLN B 484 27.442 84.198 42.532 1.00 65.59 2767 NE2 GLN B 484 27.486 86.267 43.416 1.00 62.36 2768 C CLN B 484 22.642 85.036 44.141 1.00 40.69 2769 O GLN B 484 22.503 84.476 45.232 1.00 39.56 2770 N LEU B 485 22.242 84.502 42.989 1.00 34.74 2771 CA LEU B 485 21.602 83.192 42.909 1.00 36.73 2772 CB LEU B 485 20.721 83.089 41.655 1.00 36.78 2773 CG LEU B 485 19.589 84.099 41.457 1.00 38.16 2774 CD1 LEU B 485 18.876 83.831 40.134 1.00 39.22 2775 CD2 LEU B 485 18.631 83.993 42.621 1.00 41.68 2776 C LEU B 485 22.677 82.115 42.834 1.00 36.82 2777 O LEU B 485 23.805 82.388 42.440 1.00 34.53 2778 N PRO B 486 22.342 80.875 43.217 1.00 40.02 2779 CD PRO B 486 21.037 80.349 43.652 1.00 39.74 2780 CA PRO B 486 23.351 79.809 43.151 1.00 45.08 2781 CB PRO B 486 22.606 78.582 43.678 1.00 44.97 2782 CG PRO B 486 21.438 79.143 44.439 1.00 41.94 2783 C PRO B 486 23.738 79.629 41.687 1.00 49.91 2784 O PRO B 486 22.889 79.770 40.809 1.00 49.23 2785 N ASP B 487 25.001 79.309 41.423 1.00 54.02 2786 CA ASP B 487 25.469 79.114 40.054 1.00 58.50 2787 CB ASP B 487 26.953 78.749 40.061 1.00 68.77 2788 CG ASP B 487 27.607 78.938 38.708 1.00 79.77 2789 OD1 ASP B 487 27.055 78.436 37.703 1.00 87.08 2790 OD2 ASP B 487 28.679 79.584 38.652 1.00 87.04 2791 C ASP B 487 24.672 78.006 39.354 1.00 57.99 2792 O ASP B 487 24.248 78.155 38.202 1.00 58.25 2793 N ALA B 488 24.465 76.905 40.071 1.00 55.74 2794 CA ALA B 488 23.739 75.748 39.554 1.00 55.27 2795 CB ALA B 488 23.478 74.767 40.682 1.00 55.02 2796 C ALA B 488 22.423 76.089 38.861 1.00 54.82 2797 O ALA B 488 21.874 75.274 38.117 1.00 55.09 2798 N ARG B 489 21.918 77.293 39.096 1.00 52.93 2799 CA ARG B 489 20.656 77.701 38.501 1.00 48.90 2800 CB ARG B 489 20.029 78.801 39.351 1.00 47.45 2801 CG ARG B 489 19.257 78.264 40.537 1.00 49.40 2802 CD ARG B 489 17.772 78.337 40.256 1.00 52.76 2803 NE ARG B 489 17.174 79.497 40.910 1.00 60.57 2804 CZ ARG B 489 16.041 80.087 40.540 1.00 60.40 2805 NH1 ARG B 489 15.353 79.641 39.496 1.00 61.65 2806 NH2 ARG B 489 15.587 81.120 41.234 1.00 62.45 2807 C ARG B 489 20.706 78.144 37.042 1.00 45.96 2808 O ARG B 489 19.688 78.099 36.354 1.00 45.86 2809 N HIS B 490 21.867 78.568 36.559 1.00 41.69 2810 CA HIS B 490 21.945 79.020 35.172 1.00 38.41 2811 CB HIS B 490 22.314 80.513 35.103 1.00 39.34 2812 CG HIS B 490 23.703 80.825 35.570 1.00 38.03 2813 CD2 HIS B 490 24.885 80.816 34.911 1.00 41.49 2814 ND1 HIS B 490 23.994 81.157 36.876 1.00 44.03 2815 CE1 HIS B 490 25.298 81.337 37.001 1.00 42.68 2816 NE2 HIS B 490 25.860 81.135 35.823 1.00 46.75 2817 C HIS B 490 22.921 78.218 34.322 1.00 37.56 2818 O HIS B 490 23.748 77.483 34.840 1.00 38.74 2819 N SER B 491 22.804 78.359 33.006 1.00 36.46 2820 CA SER B 491 23.694 77.674 32.079 1.00 35.63 2821 CB SER B 491 22.902 76.660 31.255 1.00 34.76 2822 OG SER B 491 23.751 75.950 30.374 1.00 51.24 2823 C SER B 491 24.355 78.712 31.165 1.00 32.46 2824 O SER B 491 23.672 79.478 30.482 1.00 34.26 2825 N THR B 492 25.681 78.732 31.154 1.00 30.35 2826 CA THR B 492 26.453 79.678 30.350 1.00 32.31 2827 CB THR B 492 27.421 80.496 31.263 1.00 33.20 2828 OG1 THR B 492 26.667 81.141 32.294 1.00 38.93 2829 CG2 THR B 492 28.185 81.554 30.478 1.00 30.28 2830 C THR B 492 27.272 78.961 29.265 1.00 32.83 2831 O THR B 492 27.930 77.962 29.535 1.00 34.30 2832 N THR B 493 27.240 79.482 28.042 1.00 32.82 2833 CA THR B 493 27.990 78.881 26.939 1.00 32.09 2834 CB THR B 493 27.449 79.346 25.570 1.00 27.96 2835 OG1 THR B 493 27.541 80.775 25.470 1.00 29.42 2836 CG2 THR B 493 26.000 78.920 25.406 1.00 21.13 2837 C THR B 493 29.469 79.264 27.033 1.00 34.06 2838 O THR B 493 29.830 80.164 27.783 1.00 31.49 2839 N GLN B 494 30.318 78.570 26.284 1.00 35.84 2840 CA GLN B 494 31.752 78.860 26.276 1.00 40.51 2841 CB GLN B 494 32.544 77.671 25.718 1.00 46.41 2842 CG GLN B 494 32.522 76.431 26.596 1.00 63.89 2843 CD GLN B 494 33.008 76.710 28.007 1.00 72.04 2844 OE1 GLN B 494 34.053 77.328 28.206 1.00 77.06 2845 NE2 GLN B 494 32.250 76.245 28.996 1.00 81.58 2846 C GLN B 494 32.004 80.088 25.409 1.00 39.51 2847 O GLN B 494 31.330 80.296 24.402 1.00 38.74 2848 N PRO B 495 32.977 80.924 25.795 1.00 38.63 2849 CD PRO B 495 33.751 80.913 27.049 1.00 37.82 2850 CA PRO B 495 33.270 82.120 25.000 1.00 39.10 2851 CB PRO B 495 34.476 82.711 25.709 1.00 37.94 2852 CG PRO B 495 34.212 82.345 27.146 1.00 43.34 2853 C PRO B 495 33.569 81.746 23.551 1.00 41.43 2854 O PRO B 495 34.254 80.762 23.292 1.00 42.40 2855 N ARG B 496 33.033 82.514 22.613 1.00 41.33 2856 CA ARG B 496 33.257 82.257 21.194 1.00 46.41 2857 CB ARG B 496 31.965 81.792 20.526 1.00 44.11 2858 CG ARG B 496 31.657 80.337 20.768 1.00 51.48 2859 CD ARG B 496 30.269 79.967 20.287 1.00 56.73 2860 NE ARG B 496 30.207 78.562 19.903 1.00 63.41 2861 CZ ARG B 496 30.616 78.093 18.727 1.00 59.61 2862 NH1 ARG B 496 31.111 78.917 17.814 1.00 60.71 2863 NH2 ARG B 496 30.534 76.796 18.466 1.00 67.27 2864 C ARG B 496 33.765 83.510 20.503 1.00 49.11 2865 O ARG B 496 33.297 84.611 20.782 1.00 48.52 2866 N LYS B 497 34.730 83.345 19.608 1.00 53.35 2867 CA LYS B 497 35.278 84.484 18.892 1.00 60.05 2868 CB LYS B 497 36.499 84.073 18.066 1.00 65.19 2869 CG LYS B 497 37.713 83.690 18.888 1.00 75.27 2870 CD LYS B 497 38.895 83.345 17.997 1.00 80.74 2871 CE LYS B 497 40.130 83.066 18.831 1.00 86.89 2872 NZ LYS B 497 41.322 82.746 17.997 1.00 91.84 2873 C LYS B 497 34.224 85.054 17.969 1.00 62.05 2874 O LYS B 497 33.209 84.416 17.697 1.00 61.50 2875 N THR B 498 34.465 86.265 17.496 1.00 66.47 2876 CA THR B 498 33.540 86.910 16.585 1.00 71.47 2877 CB THR B 498 32.946 88.183 17.207 1.00 73.54 2878 OG1 THR B 498 33.619 88.482 18.434 1.00 77.08 2879 CG2 THR B 498 31.480 87.981 17.491 1.00 75.50 2880 C THR B 498 34.281 87.261 15.306 1.00 72.65 2881 O THR B 498 35.377 86.750 15.063 1.00 72.18 2882 N ALA B 499 33.682 88.123 14.490 1.00 75.02 2883 CA ALA B 499 34.297 88.538 13.233 1.00 77.01 2884 CB ALA B 499 33.230 89.092 12.286 1.00 76.94 2885 C ALA B 499 35.376 89.591 13.493 1.00 77.96 2886 O ALA B 499 35.501 90.566 12.750 1.00 79.10 2887 N GLY B 500 36.157 89.386 14.548 1.00 78.37 2888 CA GLY B 500 37.210 90.327 14.883 1.00 78.64 2889 C GLY B 500 36.855 91.208 16.068 1.00 77.71 2890 O GLY B 500 37.722 91.859 16.653 1.00 78.53 2891 N SER B 501 35.579 91.210 16.439 1.00 76.72 2892 CA SER B 501 35.099 92.033 17.545 1.00 74.10 2893 CB SER B 501 33.707 92.583 17.201 1.00 79.09 2894 OG SER B 501 32.813 91.547 16.824 1.00 82.51 2895 C SER B 501 35.055 91.365 18.924 1.00 70.47 2896 O SER B 501 34.025 91.412 19.601 1.00 71.67 2897 N GLY B 502 36.165 90.751 19.339 1.00 64.36 2898 CA GLY B 502 36.231 90.116 20.653 1.00 55.25 2899 C GLY B 502 35.489 88.801 20.889 1.00 48.43 2900 O GLY B 502 35.445 87.931 20.019 1.00 47.45 2901 N PHE B 503 34.922 88.648 22.085 1.00 41.96 2902 CA PHE B 503 34.189 87.425 22.435 1.00 34.38 2903 CB PHE B 503 34.925 86.625 23.518 1.00 34.97 2904 CG PHE B 503 36.296 86.168 23.121 1.00 28.11 2905 CD1 PHE B 503 37.368 87.052 23.126 1.00 36.44 2906 CD2 PHE B 503 36.518 84.851 22.752 1.00 30.75 2907 CE1 PHE B 503 38.640 86.629 22.762 1.00 37.43 2908 CE2 PHE B 503 37.788 84.421 22.384 1.00 40.11 2909 CZ PHE B 503 38.850 85.311 22.391 1.00 37.06 2910 C PHE B 503 32.775 87.678 22.933 1.00 28.77 2911 O PHE B 503 32.424 88.784 23.344 1.00 28.23 2912 N PHE B 504 31.963 86.637 22.887 1.00 24.91 2913 CA PHE B 504 30.594 86.713 23.357 1.00 25.79 2914 CB PHE B 504 29.594 86.956 22.214 1.00 22.02 2915 CG PHE B 504 29.343 85.766 21.326 1.00 30.92 2916 CD1 PHE B 504 28.300 84.878 21.601 1.00 32.77 2917 CD2 PHE B 504 30.113 85.563 20.181 1.00 34.76 2918 CE1 PHE B 504 28.030 83.804 20.751 1.00 29.72 2919 CE2 PHE B 504 29.852 84.493 19.326 1.00 33.59 2920 CZ PHE B 504 28.801 83.613 19.620 1.00 34.51 2921 C PHE B 504 30.272 85.425 24.073 1.00 28.90 2922 O PHE B 504 30.849 84.378 23.783 1.00 26.02 2923 N VAL B 505 29.348 85.529 25.020 1.00 25.50 2924 CA VAL B 505 28.919 84.404 25.804 1.00 25.53 2925 CB VAL B 505 29.709 84.407 27.145 1.00 29.70 2926 CG1 VAL B 505 29.124 85.416 28.098 1.00 25.34 2927 CG2 VAL B 505 29.763 83.037 27.735 1.00 35.22 2928 C VAL B 505 27.404 84.585 26.008 1.00 26.24 2929 O VAL B 505 26.893 85.705 26.004 1.00 22.25 2930 N PHE B 506 26.687 83.475 26.150 1.00 28.62 2931 CA PHE B 506 25.239 83.507 26.346 1.00 25.84 2932 CB PHE B 506 24.539 82.831 25.165 1.00 29.19 2933 CG PHE B 506 23.053 82.811 25.273 1.00 35.82 2934 CD1 PHE B 506 22.314 83.970 25.070 1.00 42.42 2935 CD2 PHE B 506 22.387 81.639 25.600 1.00 42.16 2936 CE1 PHE B 506 20.929 83.956 25.190 1.00 44.85 2937 CE2 PHE B 506 21.009 81.618 25.724 1.00 41.56 2938 CZ PHE B 506 20.278 82.775 25.520 1.00 45.90 2939 C PHE B 506 24.881 82.756 27.627 1.00 23.92 2940 O PHE B 506 25.405 81.676 27.875 1.00 27.54 2941 N SER B 507 23.982 83.314 28.423 1.00 25.96 2942 CA SER B 507 23.559 82.675 29.668 1.00 25.75 2943 CB SER B 507 24.119 83.456 30.865 1.00 24.23 2944 OG SER B 507 23.643 82.926 32.088 1.00 33.35 2945 C SER B 507 22.026 82.573 29.736 1.00 25.49 2946 O SER B 507 21.316 83.530 29.452 1.00 25.61 2947 N ARG B 508 21.537 81.397 30.106 1.00 26.99 2948 CA ARG B 508 20.103 81.125 30.193 1.00 25.78 2949 CE ARG B 508 19.779 79.948 29.275 1.00 24.46 2950 CG ARG B 508 18.355 79.423 29.347 1.00 28.19 2951 CD ARG B 508 18.251 78.191 28.462 1.00 27.68 2952 NE ARG B 508 16.877 77.735 28.296 1.00 38.82 2953 CZ ARG B 508 16.245 76.959 29.167 1.00 40.66 2954 NH1 ARG B 508 16.874 76.554 30.260 1.00 39.61 2955 NH2 ARG B 508 14.987 76.593 28.949 1.00 40.23 2956 C ARG B 508 19.690 80.784 31.629 1.00 24.52 2957 O ARG B 508 20.366 80.006 32.290 1.00 24.88 2958 N LEU B 509 18.587 81.354 32.108 1.00 26.27 2959 CA LEU B 509 18.110 81.088 33.478 1.00 31.33 2960 CB LEU B 509 18.394 82.297 34.379 1.00 32.56 2961 CG LEU B 509 17.826 82.289 35.808 1.00 33.39 2962 CD1 LEU B 509 18.551 81.250 36.666 1.00 27.13 2963 CD2 LEU B 509 17.986 83.679 36.409 1.00 27.35 2964 C LEU B 509 16.612 80.770 33.550 1.00 33.20 2965 O LEU B 509 15.777 81.654 33.379 1.00 35.36 2966 N GLU B 510 16.270 79.509 33.814 1.00 33.43 2967 CA CLD B 510 14.865 79.121 33.918 1.00 37.45 2968 CE CLD B 510 14.720 77.598 33.795 1.00 38.70 2969 CG GLU B 510 15.248 77.052 32.471 1.00 53.61 2970 CD GLU B 510 14.878 75.591 32.203 1.00 62.03 2971 OE1 CLD B 510 15.161 74.723 33.058 1.00 65.31 2972 OE2 CLD B 510 14.310 75.312 31.124 1.00 63.62 2973 C CLD B 510 14.315 79.593 35.259 1.00 37.95 2974 O GLU B 510 14.965 79.413 36.292 1.00 35.84 2975 N VAL B 511 13.134 80.209 35.255 1.00 37.36 2976 CA VAL B 511 12.552 80.697 36.504 1.00 39.69 2977 CB VAL B 511 12.588 82.234 36.587 1.00 29.12 2978 CG1 VAL B 511 14.010 82.725 36.411 1.00 28.52 2979 CG2 VAL B 511 11.667 82.836 35.546 1.00 31.67 2980 C VAL B 511 11.110 80.243 36.708 1.00 45.51 2981 O VAL B 511 10.444 79.824 35.756 1.00 46.84 2982 N THR B 512 10.636 80.331 37.950 1.00 47.32 2983 CA THR B 512 9.274 79.927 38.287 1.00 51.20 2984 CE THR B 512 9.129 79.678 39.796 1.00 49.91 2985 OG1 THR B 512 9.458 80.877 40.508 1.00 46.57 2986 CG2 THR B 512 10.056 78.554 40.242 1.00 49.02 2987 C THR B 512 8.288 81.015 37.887 1.00 54.77 2988 O THR B 512 8.691 82.133 37.580 1.00 54.38 2989 N ARG B 513 6.998 80.684 37.894 1.00 56.48 2990 CA ARG B 513 5.958 81.645 37.535 1.00 56.58 2991 CE ARG B 513 4.574 80.991 37.597 1.00 61.58 2992 CG ARG B 513 3.570 81.570 36.611 1.00 67.62 2993 CD ARG B 513 3.294 83.034 36.879 1.00 75.58 2994 NE ARG B 513 2.863 83.743 35.678 1.00 83.06 2995 CZ ARG B 513 2.519 85.028 35.652 1.00 86.37 2996 NH1 ARG B 513 2.551 85.744 36.764 1.00 88.41 2997 NH2 ARG B 513 2.154 85.602 34.515 1.00 87.87 2998 C ARG B 513 5.997 82.817 38.500 1.00 55.15 2999 O ARG B 513 5.744 83.961 38.117 1.00 55.55 3000 N ALA B 514 6.319 82.524 39.755 1.00 55.02 3001 CA ALA B 514 6.386 83.545 40.792 1.00 53.96 3002 CB ALA B 514 6.628 82.885 42.139 1.00 53.56 3003 C ALA B 514 7.472 84.585 40.505 1.00 54.12 3004 O ALA B 514 7.187 85.781 40.419 1.00 54.41 3005 N GLU B 515 8.716 84.136 40.364 1.00 54.63 3006 CA GLU B 515 9.802 85.065 40.089 1.00 54.64 3007 CB GLU B 515 11.166 84.375 40.238 1.00 58.15 3008 CG GLU B 515 11.208 82.932 39.769 1.00 64.48 3009 CD GLU B 515 12.493 82.221 40.174 1.00 65.38 3010 OE1 GLU B 515 12.957 82.417 41.316 1.00 66.84 3011 OE2 GLU B 515 13.037 81.451 39.359 1.00 68.35 3012 C GLU B 515 9.644 85.671 38.705 1.00 54.36 3013 O GLU B 515 10.240 86.703 38.406 1.00 51.06 3014 N TRP B 516 8.831 85.037 37.863 1.00 55.85 3015 CA TRP B 516 8.585 85.557 36.524 1.00 57.10 3016 CB TRP B 516 7.845 84.538 35.653 1.00 58.50 3017 CG TRP B 516 7.950 84.874 34.194 1.00 67.12 3018 CD2 TRP B 516 6.940 85.472 33.374 1.00 68.04 3019 CE2 TRP B 516 7.509 85.685 32.101 1.00 71.07 3020 CE3 TRP B 516 5.608 85.849 33.593 1.00 74.06 3021 CG1 TRP B 516 9.059 84.749 33.403 1.00 67.58 3022 NE1 TRP B 516 8.803 85.236 32.146 1.00 68.75 3023 CZ2 TRP B 516 6.793 86.263 31.048 1.00 75.59 3024 CZ3 TRP B 516 4.895 86.425 32.542 1.00 76.50 3025 CH2 TRP B 516 5.491 86.625 31.287 1.00 76.13 3026 C TRP B 516 7.746 86.828 36.648 1.00 57.68 3027 O TRP B 516 7.775 87.691 35.773 1.00 57.71 3028 N GLU B 517 6.996 86.935 37.743 1.00 58.53 3029 CA GLU B 517 6.173 88.113 38.008 1.00 60.83 3030 CB GLU B 517 5.219 87.842 39.179 1.00 65.68 3031 CG GLU B 517 3.832 87.363 38.775 1.00 77.69 3032 CD GLU B 517 3.078 88.387 37.932 1.00 86.61 3033 OE1 GLU B 517 3.564 89.534 37.799 1.00 92.24 3034 OE2 GLU B 517 1.995 88.050 37.404 1.00 89.43 3035 C GLU B 517 7.053 89.323 38.345 1.00 58.89 3036 O GLU B 517 6.729 90.465 38.012 1.00 56.98 3037 N ALA B 518 8.170 89.063 39.016 1.00 58.33 3038 CA ALA B 518 9.097 90.121 39.398 1.00 54.78 3039 CB ALA B 518 9.422 90.005 40.880 1.00 55.11 3040 C ALA B 518 10.373 90.003 38.560 1.00 53.56 3041 O ALA B 518 11.480 90.225 39.055 1.00 52.54 3042 N LYS B 519 10.219 89.681 37.281 1.00 51.73 3043 CA LYS B 519 11.383 89.508 36.429 1.00 52.62 3044 CB LYS B 519 10.983 88.881 35.096 1.00 52.68 3045 CG LYS B 519 10.253 89.792 34.146 1.00 53.71 3046 CD LYS B 519 9.696 88.969 32.997 1.00 61.43 3047 CE LYS B 519 8.899 89.819 32.036 1.00 65.64 3048 NZ LYS B 519 8.140 88.958 31.098 1.00 74.93 3049 C LYS B 519 12.160 90.786 36.185 1.00 52.55 3050 O LYS B 519 13.313 90.743 35.761 1.00 49.84 3051 N ASP B 520 11.533 91.920 36.462 1.00 54.27 3052 CA ASP B 520 12.176 93.219 36.280 1.00 55.54 3053 CB ASP B 520 11.146 94.337 36.431 1.00 65.40 3054 CG ASP B 520 9.722 93.857 36.196 1.00 75.80 3055 OD1 ASP B 520 9.426 93.383 35.076 1.00 83.22 3056 OD2 ASP B 520 8.900 93.948 37.136 1.00 77.87 3057 C ASP B 520 13.255 93.388 37.346 1.00 53.46 3058 O ASP B 520 14.100 94.281 37.257 1.00 51.37 3059 N GLU B 521 13.217 92.521 38.353 1.00 50.72 3060 CA GLU B 521 14.178 92.584 39.442 1.00 50.66 3061 CB GLU B 521 13.507 92.173 40.758 1.00 54.68 3062 CG GLU B 521 12.510 93.192 41.301 1.00 61.75 3063 CD GLU B 521 11.663 92.639 42.430 1.00 68.36 3064 OE1 GLU B 521 12.232 92.137 43.422 1.00 70.14 3065 OE2 GLU B 521 10.419 92.708 42.327 1.00 75.93 3066 C GLU B 521 15.418 91.731 39.215 1.00 46.52 3067 O GLU B 521 16.392 91.857 39.952 1.00 47.21 3068 N PHE B 522 15.386 90.866 38.207 1.00 42.97 3069 CA PHE B 522 16.531 90.011 37.919 1.00 38.46 3070 CB PHE B 522 16.091 88.752 37.185 1.00 37.28 3071 CG PHE B 522 15.420 87.754 38.076 1.00 42.52 3072 CD1 PHE B 522 14.090 87.925 38.454 1.00 44.12 3073 CD2 PHE B 522 16.133 86.671 38.592 1.00 40.14 3074 CE1 PHE B 522 13.474 87.036 39.338 1.00 48.02 3075 CE2 PHE B 522 15.528 85.775 39.477 1.00 42.77 3076 CZ PHE B 522 14.192 85.960 39.852 1.00 41.32 3077 C PHE B 522 17.594 90.748 37.130 1.00 36.02 3078 O PHE B 522 17.292 91.474 36.182 1.00 37.87 3079 N ILE B 523 18.842 90.558 37.539 1.00 32.13 3080 CA ILE B 523 19.974 91.224 36.913 1.00 31.74 3081 CB ILE B 523 20.634 92.208 37.908 1.00 36.58 3082 CG2 ILE B 523 21.849 92.889 37.262 1.00 38.36 3083 CG1 ILE B 523 19.600 93.233 38.386 1.00 39.38 3084 CD1 ILE B 523 20.086 94.083 39.536 1.00 40.35 3085 C ILE B 523 21.041 90.244 36.430 1.00 30.51 3086 O ILE B 523 21.306 89.231 37.066 1.00 29.34 3087 N CYS B 524 21.651 90.554 35.298 1.00 28.73 3088 CA CYS B 524 22.702 89.721 34.749 1.00 27.60 3089 C CYS B 524 23.965 90.519 34.964 1.00 27.54 3090 O CYS B 524 24.033 91.667 34.545 1.00 28.72 3091 CB CYS B 524 22.477 89.504 33.251 1.00 26.75 3092 SG CYS B 524 23.823 88.601 32.411 1.00 36.31 3093 N ARG B 525 24.964 89.925 35.603 1.00 28.42 3094 CA ARG B 525 26.200 90.634 35.874 1.00 28.35 3095 CB ARG B 525 26.371 90.820 37.380 1.00 34.16 3096 CG ARG B 525 27.688 91.480 37.769 1.00 39.75 3097 CD ARG B 525 27.604 92.092 39.163 1.00 48.43 3098 NE ARG B 525 27.775 91.117 40.226 1.00 52.97 3099 CZ ARG B 525 27.492 91.358 41.502 1.00 58.72 3100 NE1 ARG B 525 27.020 92.546 41.867 1.00 55.56 3101 NE2 ARG B 525 27.670 90.410 42.414 1.00 55.90 3102 C ARG B 525 27.416 89.927 35.317 1.00 28.14 3103 O ARG B 525 27.545 88.711 35.409 1.00 28.95 3104 N ALA B 526 28.317 90.708 34.743 1.00 25.82 3105 CA ALA B 526 29.518 90.160 34.170 1.00 25.90 3106 CB ALA B 526 29.614 90.544 32.691 1.00 28.82 3107 C ALA B 526 30.697 90.729 34.931 1.00 27.38 3108 O ALA B 526 30.701 91.910 35.253 1.00 24.32 3109 N VAL B 527 31.676 89.882 35.245 1.00 24.37 3110 CA VAL B 527 32.873 90.334 35.923 1.00 24.12 3111 CB VAL B 527 33.166 89.546 37.201 1.00 24.30 3112 CG1 VAL B 527 34.510 89.963 37.762 1.00 26.10 3113 CG2 VAL B 527 32.083 89.804 38.224 1.00 30.97 3114 C VAL B 527 33.954 90.077 34.902 1.00 26.78 3115 O VAL B 527 34.078 88.969 34.375 1.00 25.10 3116 N HIS B 528 34.743 91.103 34.630 1.00 26.18 3117 CA HIS B 528 35.771 91.015 33.616 1.00 29.17 3118 CB HIS B 528 35.110 91.187 32.221 1.00 28.69 3119 CG HIS B 528 36.078 91.191 31.072 1.00 30.83 3120 CD2 HIS B 528 36.939 92.144 30.639 1.00 30.29 3121 ND1 HIS B 528 36.282 90.096 30.258 1.00 30.55 3122 CE1 HIS B 528 37.233 90.372 29.381 1.00 28.76 3123 NE2 HIS B 528 37.650 91.608 29.593 1.00 23.82 3124 C HIS B 528 36.818 92.102 33.870 1.00 31.62 3125 O HIS B 528 36.504 93.213 34.312 1.00 30.62 3126 N GLU B 529 38.061 91.766 33.557 1.00 34.89 3127 CA GLU B 529 39.200 92.651 33.753 1.00 41.27 3128 CB GLU B 529 40.471 91.960 33.257 1.00 46.90 3129 CG GLU B 529 41.692 92.879 33.228 1.00 61.52 3130 CD GLU B 529 42.764 92.416 32.248 1.00 68.52 3131 OE1 GLU B 529 43.740 93.167 32.036 1.00 68.05 3132 OE2 GLU B 529 42.631 91.306 31.687 1.00 73.22 3133 C GLU B 529 39.124 94.035 33.104 1.00 42.79 3134 O GLU B 529 39.531 95.022 33.719 1.00 42.08 3135 N ALA B 530 38.622 94.098 31.868 1.00 43.28 3136 CA ALA B 530 38.539 95.350 31.113 1.00 44.89 3137 CB ALA B 530 38.417 95.054 29.628 1.00 42.67 3138 C ALA B 530 37.458 96.337 31.518 1.00 47.12 3139 O ALA B 530 37.463 97.474 31.052 1.00 47.05 3140 N ALA B 531 36.529 95.916 32.368 1.00 50.02 3141 CA ALA B 531 35.470 96.808 32.820 1.00 54.71 3142 CB ALA B 531 34.367 95.998 33.479 1.00 52.38 3143 C ALA B 531 36.081 97.813 33.808 1.00 59.71 3144 O ALA B 531 35.765 97.816 34.998 1.00 57.91 3145 N SER B 532 36.958 98.664 33.275 1.00 66.39 3146 CA SER B 532 37.701 99.689 34.022 1.00 71.61 3147 CB SER B 532 37.651 101.030 33.272 1.00 75.15 3148 OG SER B 532 36.326 101.410 32.932 1.00 81.74 3149 C SER B 532 37.402 99.919 35.505 1.00 73.08 3150 O SER B 532 38.293 99.745 36.343 1.00 75.98 3151 N PRO B 533 36.167 100.321 35.864 1.00 72.21 3152 CD PRO B 533 35.011 100.831 35.102 1.00 72.93 3153 CA PRO B 533 35.956 100.524 37.299 1.00 69.88 3154 CB PRO B 533 34.983 101.687 37.325 1.00 69.60 3155 CG PRO B 533 34.063 101.322 36.205 1.00 71.96 3156 C PRO B 533 35.388 99.283 37.987 1.00 67.12 3157 O PRO B 533 34.331 98.780 37.600 1.00 67.77 3158 N SER B 534 36.101 98.798 38.997 1.00 62.96 3159 CA SER B 534 35.683 97.633 39.769 1.00 56.20 3160 CB SER B 534 34.463 97.991 40.621 1.00 57.74 3161 OG SER B 534 33.463 98.615 39.838 1.00 67.85 3162 C SER B 534 35.406 96.342 38.989 1.00 49.03 3163 O SER B 534 34.789 95.424 39.524 1.00 47.21 3164 N CLN B 535 35.858 96.278 37.737 1.00 42.33 3165 CA GUN B 535 35.704 95.096 36.896 1.00 38.93 3166 CB GLN B 535 36.713 94.012 37.316 1.00 32.30 3167 CG GUN B 535 38.181 94.388 37.128 1.00 35.25 3168 CD GLN B 535 38.619 95.526 38.024 1.00 41.01 3169 OE1 GLN B 535 38.428 95.488 39.239 1.00 43.29 3170 NE2 GLN B 535 39.220 96.545 37.431 1.00 47.79 3171 C GLN B 535 34.310 94.485 36.891 1.00 37.85 3172 O GLN B 535 34.168 93.265 36.819 1.00 36.76 3173 N THR B 536 33.283 95.320 36.953 1.00 37.28 3174 CA THR B 536 31.925 94.805 36.955 1.00 39.00 3175 CB THR B 536 31.319 94.848 38.366 1.00 41.53 3176 OG1 THR B 536 32.267 94.344 39.314 1.00 46.75 3177 CG2 THR B 536 30.076 93.987 38.424 1.00 39.44 3178 C THR B 536 31.016 95.586 36.028 1.00 38.42 3179 O THR B 536 31.148 96.794 35.895 1.00 43.26 3180 N VAL B 537 30.105 94.877 35.374 1.00 37.42 3181 CA VAL B 537 29.131 95.462 34.468 1.00 32.52 3182 CB VAL B 537 29.619 95.466 32.990 1.00 36.29 3183 CG1 VAL B 537 28.580 96.148 32.114 1.00 35.71 3184 CG2 VAL B 537 30.931 96.205 32.859 1.00 43.42 3185 C VAL B 537 27.876 94.594 34.562 1.00 31.41 3186 O VAL B 537 27.946 93.369 34.435 1.00 31.67 3187 N GLN B 538 26.726 95.219 34.787 1.00 27.91 3188 CA GLN B 538 25.496 94.452 34.917 1.00 29.41 3189 CB GLN B 538 25.231 94.136 36.392 1.00 29.17 3190 CG GLN B 538 24.965 95.363 37.251 1.00 29.81 3191 CD GLN B 538 24.710 94.983 38.691 1.00 29.58 3192 OE1 GLN B 538 25.443 94.176 39.267 1.00 37.40 3193 NE2 GLN B 538 23.676 95.559 39.285 1.00 32.13 3194 C GLN B 538 24.304 95.193 34.356 1.00 31.40 3195 O CLN B 538 24.314 96.411 34.256 1.00 33.62 3196 N ARG B 539 23.267 94.449 34.002 1.00 31.64 3197 CA ARG B 539 22.066 95.063 33.481 1.00 34.86 3198 CB ARG B 539 22.120 95.120 31.955 1.00 41.64 3199 CG ARG B 539 21.123 96.078 31.338 1.00 48.95 3200 CD ARG B 539 21.796 96.845 30.216 1.00 59.63 3201 NE ARG B 539 23.067 97.395 30.680 1.00 74.02 3202 CZ ARG B 539 23.909 98.094 29.927 1.00 82.05 3203 NH1 ARG B 539 23.623 98.341 28.653 1.00 87.03 3204 NH2 ARG B 539 25.040 98.547 30.454 1.00 85.40 3205 C ARG B 539 20.840 94.289 33.922 1.00 34.74 3206 O ARG B 539 20.833 93.059 33.910 1.00 37.29 3207 N ALA B 540 19.806 95.020 34.328 1.00 34.85 3208 CA ALA B 540 18.561 94.408 34.756 1.00 34.24 3209 CB ALA B 540 17.709 95.425 35.472 1.00 35.02 3210 C ALA B 540 17.846 93.900 33.513 1.00 35.51 3211 O ALA B 540 18.082 94.395 32.405 1.00 30.77 3212 N VAL B 541 16.996 92.896 33.692 1.00 36.19 3213 CA VAL B 541 16.251 92.326 32.580 1.00 42.85 3214 CB VAL B 541 15.335 91.172 33.062 1.00 43.71 3215 CG1 VAL B 541 14.284 90.856 32.016 1.00 48.75 3216 CG2 VAL B 541 16.167 89.935 33.351 1.00 43.59 3217 C VAL B 541 15.406 93.419 31.922 1.00 48.00 3218 O VAL B 541 14.537 94.013 32.564 1.00 44.96 3219 N SER B 542 15.673 93.694 30.649 1.00 53.41 3220 CA SER B 542 14.914 94.717 29.948 1.00 61.94 3221 CB SER B 542 15.564 95.068 28.606 1.00 62.96 3222 OG SER B 542 15.462 94.004 27.679 1.00 69.91 3223 C SER B 542 13.517 94.163 29.728 1.00 65.98 3224 O SER B 542 13.347 92.972 29.466 1.00 67.12 3225 N VAL B 543 12.520 95.029 29.851 1.00 70.21 3226 CA VAL B 543 11.134 94.625 29.679 1.00 74.63 3227 CB VAL B 543 10.479 94.300 31.042 1.00 78.23 3228 CG1 VAL B 543 9.026 93.887 30.840 1.00 79.65 3229 CG2 VAL B 543 11.256 93.191 31.741 1.00 79.80 3230 C VAL B 543 10.341 95.729 28.989 1.00 75.67 3231 O VAL B 543 9.847 96.626 29.704 1.00 77.58 3232 OXT VAL B 543 10.240 95.693 27.744 1.00 74.95 3233 C1 NAG B 2 34.354 65.734 31.802 1.00 97.60 3234 O1 NAG B 2 33.245 65.687 30.975 1.00 99.81 3235 C2 NAG B 2 34.505 67.148 32.413 1.00 96.75 3236 N2 NAG B 2 33.295 67.525 33.111 1.00 98.55 3237 C7 NAG B 2 33.264 67.560 34.440 1.00 101.24 3238 O7 NAG B 2 34.215 67.219 35.144 1.00 100.19 3239 C8 NAG B 2 31.977 68.033 35.094 1.00 100.76 3240 C3 NAG B 2 34.781 68.206 31.328 1.00 96.21 3241 O3 NAG B 2 35.075 69.462 31.938 1.00 95.30 3242 C4 NAG B 2 35.966 67.760 30.458 1.00 94.75 3243 O4 NAG B 2 36.156 68.676 29.375 1.00 91.92 3244 C5 NAG B 2 3S.704 66.327 29.921 1.00 95.52 324S O5 NAG B 2 35.S07 6S.396 31.017 1.00 96.34 3246 C6 NAG B 2 36.873 6S.82S 29.101 1.00 96.13 3247 O6 NAG B 2 38.093 65.877 29.834 1.00 99.34 3248 OH2 TIP B 1 28.270 80.979 34.917 1.00 50.26 3249 OH2 TIP B 2 50.798 88.311 45.038 1.00 49.71 3250 OH2 TIP B 3 16.542 94.946 50.298 1.00 62.73 3251 OH2 TIP B 4 24.725 83.256 39.944 1.00 44.66 3252 OH2 TIP B 5 40.269 78.063 37.8S1 1.00 53.56 3253 OH2 TIP B 6 9.197 79.408 26.351 1.00 44.98 3254 OH2 TIP B 7 26.398 96.745 29.206 1.00 44.08 3255 OH2 TIP B 8 38.618 89.009 32.579 1.00 40.39 3256 OH2 TIP B 9 39.672 81.166 40.426 1.00 40.49 3257 OH2 TIP B 10 17.116 78.215 37.161 1.00 46.89 3258 OH2 TIP B 11 18.243 77.296 33.917 1.00 50.51 3259 OH2 TIP B 12 27.078 76.693 33.012 1.00 50.17 3260 OH2 TIP B 13 35.090 58.030 33.714 1.00 54.70 3261 OH2 TIP B 14 29.218 81.786 23.355 1.00 44.57 3262 OH2 TIP B 15 43.924 82.629 46.436 1.00 50.94 3263 OH2 TIP B 16 1.538 85.984 28.824 1.00 56.21 3264 OH2 TIP B 17 30.S90 75.306 16.280 1.00 59.52 3265 OH2 TIP B 18 23.180 95.510 42.272 1.00 55.58 3266 OH2 TIP B 19 32.511 60.357 37.976 1.00 66.56 3267 OH2 TIP B 20 34.997 58.857 36.088 1.00 63.77 3268 OH2 TIP B 21 13.039 76.542 38.487 1.00 62.34 3269 OH2 TIP B 22 46.374 79.044 30.275 1.00 54.44 3270 OH2 TIP B 23 50.931 79.559 44.881 1.00 52.42 3271 OH2 TIP B 24 37.386 70.634 30.326 1.00 60.14 3272 OH2 TIP B 25 49.964 85.552 35.048 1.00 48.11 3273 OH2 TIP B 26 19.519 76.770 31.435 1.00 45.10 3274 OH2 TIP B 27 36.515 71.442 28.12S 1.00 59.32 3275 OH2 TIP B 28 S8.S06 76.725 41.675 1.00 53.61 3276 OH2 TIP B 29 38.094 79.042 44.064 1.00 60.13 3277 OH2 TIP B 30 52.870 67.201 28.126 1.00 56.34 3278 OH2 TIP B 31 33.4S6 82.100 36.961 1.00 58.14 3279 OH2 TIP B 32 40.793 70.829 43.558 1.00 50.57 3280 OH2 TIP B 33 9.876 81.332 43.156 1.00 56.48 3281 OH2 TIP B 34 26.776 77.910 3S.274 1.00 60.64 3282 OH2 TIP B 35 32.082 S6.279 37.927 1.00 56.7S 3283 OH2 TIP B 36 41.915 8S.209 33.986 1.00 S2.49 3284 OH2 TIP B 37 35.082 80.384 18.510 1.00 56.17 3285 OH2 TIP B 38 57.244 63.192 22.89S 1.00 S7.49 3286 OH2 TIP B 39 6.333 76.420 30.801 1.00 S9.27 3287 OH2 TIP B 40 29.685 90.602 44.591 1.00 SS.17 3288 OH2 TIP B 41 36.388 79.659 25.044 1.00 55.25 3289 OH2 TIP B 42 19.034 94.293 29.572 1.00 50.93 3290 OH2 TIP B 43 40.676 79.023 31.687 1.00 58.05 3291 OH2 TIP B 44 29.928 96.295 23.009 1.00 63.22 3292 OH2 TIP B 45 14.498 74.337 37.588 1.00 59.76 3293 OH2 TIP B 46 34.047 76.484 31.577 1.00 61.09 3294 OH2 TIP B 47 55.169 85.314 45.805 1.00 58.75 3295 OH2 TIP B 48 48.047 66.430 43.800 1.00 59.73 3296 OH2 TIP B 49 33.940 96.758 23.804 1.00 53.77 3297 OH2 TIP B 50 57.073 93.041 37.538 1.00 59.31 3298 OH2 TIP B 51 29.485 77.394 32.123 1.00 56.85 3299 OH2 TIP B 52 28.540 96.775 19.917 1.00 60.05 3300 OH2 TIP B 53 44.894 72.951 29.410 1.00 57.10 3301 OH2 TIP B 54 45.362 55.938 33.103 1.00 60.54 3302 OH2 TIP B 55 48.139 75.237 29.289 1.00 62.47 3303 OH2 TIP B 56 1.034 81.059 27.240 1.00 64.33 3304 OH2 TIP B 57 35.432 94.188 20.969 1.00 52.42 3305 OH2 TIP B 58 17.286 95.575 43.504 1.00 60.20 3306 OH2 TIP B 59 41.972 83.557 20.901 1.00 59.26 3307 OH2 TIP B 60 29.469 59.186 40.661 1.00 62.09 3308 OH2 TIP B 61 51.530 82.833 43.577 1.00 65.16 3309 OH2 TIP B 62 26.641 90.990 45.263 1.00 59.85 3310 OH2 TIP B 63 46.399 87.498 46.342 1.00 56.88 3311 OH2 TIP B 64 25.335 75.984 42.835 1.00 53.06 3312 OH2 TIP B 65 8.193 87.217 28.036 1.00 60.26 3313 OH2 TIP B 66 28.032 88.745 44.846 1.00 59.03 3314 OH2 TIP B 67 40.713 72.843 34.794 1.00 54.95 3315 OH2 TIP B 68 8.183 78.374 34.568 1.00 57.65 3316 OH2 TIP B 69 38.121 88.788 17.047 1.00 59.41 3317 OH2 TIP B 70 40.671 93.547 43.325 1.00 62.27 3318 OH2 TIP B 71 31.413 68.974 32.122 1.00 55.86 3319 OH2 TIP B 72 51.257 72.484 46.323 1.00 59.39 3320 OH2 TIP B 73 30.484 83.899 40.314 1.00 59.25 3321 OH2 TIP B 74 55.561 71.680 37.852 1.00 53.17 3322 OH2 TIP B 75 53.223 94.913 42.289 1.00 65.55 3323 OH2 TIP B 76 55.467 63.809 25.190 1.00 62.05 3324 OH2 TIP B 77 31.319 66.997 30.418 1.00 57.87 3325 OH2 TIP B 78 29.297 94.140 18.414 1.00 58.31 3326 OH2 TIP B 79 9.882 83.094 29.532 1.00 53.97 3327 OH2 TIP B 80 55.788 84.688 33.186 1.00 54.45 3328 OH2 TIP B 81 14.402 84.006 43.396 1.00 60.50 3329 OH2 TIP B 82 21.401 99.644 31.527 1.00 54.25 3330 OH2 TIP B 83 38.747 99.305 29.133 1.00 58.03 3331 OH2 TIP B 84 36.701 91.635 49.414 1.00 61.54 3332 OH2 TIP B 85 53.184 73.221 55.411 1.00 71.84 3333 OH2 TIP B 86 54.962 57.175 32.829 1.00 59.92 3334 OH2 TIP B 87 37.795 94.920 41.465 1.00 55.82 3335 OH2 TIP B 88 47.047 68.720 45.430 1.00 57.31 3336 OH2 TIP B 89 53.386 88.730 45.407 1.00 58.45 3337 OH2 TIP B 90 12.966 80.192 43.065 1.00 58.03 3338 OH2 TIP B 91 25.222 92.505 24.772 1.00 50.36 3339 OH2 TIP B 92 56.971 75.837 46.165 1.00 57.19 3340 OH2 TIP B 93 52.883 57.456 41.616 1.00 62.27 3341 OH2 TIP B 94 21.647 72.884 37.586 1.00 61.49 3342 OH2 TIP B 95 53.819 55.355 36.996 1.00 66.72 3343 OH2 TIP B 96 1.978 86.114 32.124 1.00 62.93 3344 OH2 TIP B 97 3.673 88.829 34.679 1.00 59.08 3345 OH2 TIP B 98 50.288 52.210 35.596 1.00 66.54 3346 OH2 TIP B 99 53.869 54.763 33.809 1.00 64.16 3347 OH2 TIP B 100 39.796 81.619 49.309 1.00 59.09 3348 OH2 TIP B 101 27.537 82.048 39.451 1.00 59.99 3349 OH2 TIP B 102 36.131 103.395 30.948 1.00 63.48 3350 OH2 TIP B 103 56.043 76.714 32.065 1.00 60.94 3351 OH2 TIP B 104 31.838 89.133 20.071 1.00 57.13 3352 OH2 TIP B 105 49.027 92.881 29.882 1.00 67.01 3353 OH2 TIP B 106 52.660 69.955 44.183 1.00 61.12 3354 OH2 TIP B 107 57.992 83.903 35.849 1.00 62.98 3355 OH2 TIP B 108 35.733 75.725 27.339 1.00 63.30 3356 OH2 TIP B 109 40.575 98.578 26.825 1.00 57.78 3357 OH2 TIP B 110 47.643 81.928 28.944 1.00 65.34 3358 OH2 TIP B 111 5.312 87.158 27.438 1.00 56.09 3359 OH2 TIP B 112 49.841 88.326 23.196 1.00 62.75 3360 OH2 TIP B 113 6.598 93.132 35.325 1.00 58.88 3361 OH2 TIP B 114 27.092 100.653 31.174 1.00 63.28 3362 OH2 TIP B 115 42.024 53.749 39.435 1.00 65.61 3363 OH2 TIP B 116 50.539 76.914 27.922 1.00 60.98 3364 OH2 TIP B 117 47.538 92.256 33.656 1.00 60.98 3365 OH2 TIP B 118 5.166 74.252 29.209 1.00 58.25 3366 OH2 TIP B 119 38.217 72.245 31.919 1.00 55.39 3367 OH2 TIP B 120 32.252 55.236 35.199 1.00 56.80 3368 OH2 TIP B 121 32.670 57.598 33.803 1.00 61.15 3369 OH2 TIP B 122 17.786 96.981 50.771 1.00 55.82 3370 OH2 TIP B 123 40.380 77.020 40.041 1.00 45.14 3371 OH2 TIP B 124 42.038 88.110 33.725 1.00 55.49 3372 OH2 TIP B 125 34.758 55.495 34.823 1.00 66.22 3373 OH2 TIP B 126 37.737 77.084 41.644 1.00 57.00 3374 OH2 TIP B 127 29.699 98.301 28.668 1.00 57.60 3375 OH2 TIP B 128 49.020 89.370 46.224 1.00 56.82 3376 OH2 TIP B 129 52.859 75.885 25.996 1.00 62.05 3377 OH2 TIP B 130 30.010 59.209 36.597 1.00 66.31 3378 OH2 TIP B 131 30.914 96.977 25.231 1.00 57.71 3379 OH2 TIP B 132 39.916 79.723 47.627 1.00 61.64 3380 OH2 TIP B 133 44.108 57.405 44.718 1.00 61.06 3381 OH2 TIP B 134 9.863 79.457 23.833 1.00 61.78 3382 OH2 TIP B 135 38.917 86.317 18.760 1.00 57.35 3383 OH2 TIP B 136 30.862 81.856 35.179 1.00 54.03 3384 OH2 TIP B 137 53.704 70.947 53.894 1.00 64.00 3385 OH2 TIP B 138 40.859 81.838 22.227 1.00 65.85 3386 OH2 TIP B 139 37.816 96.128 20.409 1.00 60.91 3387 OH2 TIP B 140 25.705 74.474 33.305 1.00 61.62 3388 OH2 TIP B 141 30.005 54.298 36.646 1.00 62.13 3389 OH2 TIP B 142 10.624 79.976 28.177 1.00 58.14 3390 OH2 TIP B 143 29.498 59.385 43.076 1.00 61.05 3391 OH2 TIP B 144 40.320 90.895 16.086 1.00 55.65 3392 OH2 TIP B 145 55.724 66.531 26.778 1.00 64.64 3393 OH2 TIP B 146 50.659 94.738 31.683 1.00 61.54 3394 OH2 TIP B 147 3.656 85.417 24.832 1.00 59.07 3395 OH2 TIP B 148 16.265 75.893 38.242 1.00 60.79 3396 OH2 TIP B 149 31.777 95.407 41.590 1.00 57.59 3397 OH2 TIP B 150 54.287 76.248 53.590 1.00 63.92 3398 OH2 TIP B 151 33.491 79.601 16.793 1.00 62.67 3399 OH2 TIP B 152 19.155 94.756 51.118 1.00 68.07 3400 OH2 TIP B 153 35.245 75.050 34.131 1.00 61.87 3401 OH2 TIP B 154 56.335 76.647 34.751 1.00 66.95 3402 OH2 TIP B 155 55.588 94.784 38.616 1.00 59.56 3403 OH2 TIP B 156 36.064 78.257 16.816 1.00 59.20 3404 OH2 TIP B 157 55.289 57.324 36.670 1.00 67.18 3405 OH2 TIP B 158 38.244 95.684 44.137 1.00 59.37 3406 OH2 TIP B 159 1.406 80.766 24.793 1.00 65.79 3407 OH2 TIP B 160 46.599 89.854 33.493 1.00 58.89 3408 OH2 TIP B 161 31.235 73.902 14.323 1.00 59.68 3409 OH2 TIP B 162 49.265 83.710 48.164 1.00 63.91 3410 OH2 TIP B 163 12.493 91.314 27.537 1.00 58.95 3411 OH2 TIP B 164 30.439 81.890 41.630 1.00 64.19 3412 OH2 TIP B 165 33.579 81.394 39.388 1.00 55.30 3413 OH2 TIP B 166 23.628 85.041 47.763 1.00 55.04 3414 OH2 TIP B 167 37.026 77.530 29.328 1.00 61.56 3415 OH2 TIP B 168 42.191 47.686 40.363 1.00 63.55 3416 OH2 TIP B 169 48.389 87.260 21.330 1.00 62.46 3417 OH2 TIP B 170 1.110 78.818 28.205 1.00 61.28 3418 OH2 TIP B 171 30.316 77.346 15.355 1.00 59.15 3419 OH2 TIP B 172 56.892 58.723 34.712 1.00 66.69 3420 OH2 TIP B 173 38.573 89.823 51.022 1.00 60.64 3421 OH2 TIP B 174 55.700 73.403 29.957 1.00 64.56 3422 OH2 TIP B 175 2.131 82.160 29.752 1.00 59.77 3423 OH2 TIP B 176 48.652 75.463 25.876 1.00 61.95 3424 OH2 TIP B 177 13.930 79.132 45.787 1.00 63.68 3425 OH2 TIP B 178 49.048 79.772 28.026 1.00 62.71 3426 OH2 TIP B 179 50.873 71.018 26.463 1.00 64.40 3427 OH2 TIP B 180 0.222 87.613 28.898 1.00 64.94 3428 OH2 TIP B 181 36.716 99.478 26.710 1.00 60.70 3429 OH2 TIP B 182 55.733 96.794 42.680 1.00 62.42 3430 OH2 TIP B 183 32.962 78.288 30.566 1.00 65.26 3431 OH2 TIP B 184 50.072 74.531 27.875 1.00 58.49 3432 OH2 TIP B 185 4.066 80.299 25.717 1.00 66.38 3433 OH2 TIP B 186 51.785 82.993 46.037 1.00 66.62 3434 OH2 TIP B 187 6.687 89.453 25.800 1.00 63.72 3435 OH2 TIP B 188 3.415 87.824 28.810 1.00 62.49 3436 OH2 TIP B 189 58.432 73.821 42.739 1.00 63.23 3437 OH2 TIP B 190 3.604 89.517 32.202 1.00 65.15 3438 OH2 TIP B 191 36.662 69.392 26.901 1.00 63.27 3439 OH2 TIP B 192 51.020 69.014 46.306 1.00 61.81 3440 OH2 TIP B 193 34.827 72.790 27.053 1.00 59.78 3441 OH2 TIP B 194 38.979 97.644 41.760 1.00 60.91 3442 OH2 TIP B 195 25.438 89.346 46.679 1.00 61.51

[0041] Another embodiment of the present invention is a 3-D model of a Fc-Cε3/Cε4 region that substantially represents the atomic coordinates specified (i.e., listed) in Table 2. TABLE 2 Atomic coordinates of 1FP5_dimer.pdb ATOM ATOM # TYPE RES CHN # X Y Z OCC B 1 N VAL A 336 46.157 62.618 17.991 1.00 58.93 2 CA VAL A 336 45.400 61.812 16.993 1.00 60.44 3 C VAL A 336 44.013 61.427 17.501 1.00 60.07 4 O VAL A 336 43.847 60.389 18.142 1.00 61.48 5 CB VAL A 336 46.155 60.521 16.647 1.00 60.81 6 CG1 VAL A 336 45.464 59.806 15.500 1.00 61.71 7 CG2 VAL A 336 47.590 60.845 16.302 1.00 64.73 8 N SER A 337 43.017 62.257 17.209 1.00 57.95 9 CA SER A 337 41.655 61.983 17.648 1.00 56.60 10 C SER A 337 40.683 61.842 16.476 1.00 55.17 11 O SER A 337 40.981 62.262 15.352 1.00 54.55 12 CB SER A 337 41.185 63.078 18.603 1.00 57.92 13 OG SER A 337 41.489 64.356 18.087 1.00 64.70 14 N ALA A 338 39.527 61.238 16.743 1.00 52.40 15 CA ALA A 338 38.522 61.010 15.711 1.00 50.69 16 C ALA A 338 37.109 61.300 16.192 1.00 50.25 17 O ALA A 338 36.772 61.062 17.354 1.00 51.17 18 CB ALA A 338 38.611 59.573 15.211 1.00 50.21 19 N TYR A 339 36.281 61.808 15.284 1.00 48.22 20 CA TYR A 339 34.899 62.139 15.605 1.00 46.82 21 C TYR A 339 33.990 61.766 14.431 1.00 44.51 22 O TYR A 339 34.372 61.889 13.268 1.00 42.27 23 CB TYR A 339 34.765 63.638 15.915 1.00 50.52 24 CG TYR A 339 35.869 64.198 16.793 1.00 58.40 25 CD1 TYR A 339 37.144 64.445 16.274 1.00 61.23 26 CD2 TYR A 339 35.648 64.456 18.151 1.00 60.99 27 CE1 TYR A 339 38.174 64.929 17.081 1.00 62.71 28 CE2 TYR A 339 36.674 64.943 18.969 1.00 63.53 29 CZ TYR A 339 37.933 65.176 18.427 1.00 64.33 30 OH TYR A 339 38.953 65.644 19.230 1.00 65.07 31 N LEU A 340 32.793 61.291 14.746 1.00 41.90 32 CA LEU A 340 31.831 60.905 13.728 1.00 41.06 33 C LEU A 340 30.571 61.671 14.078 1.00 41.10 34 O LEU A 340 30.136 61.647 15.224 1.00 43.45 35 CB LEU A 340 31.583 59.392 13.779 1.00 36.93 36 CG LEU A 340 30.689 58.770 12.701 1.00 35.91 37 CD1 LEU A 340 31.229 59.100 11.314 1.00 34.60 38 CD2 LEU A 340 30.621 57.264 12.906 1.00 35.51 39 N SER A 341 29.990 62.368 13.108 1.00 39.82 40 CA SER A 341 28.790 63.152 13.385 1.00 39.85 41 C SER A 341 27.598 62.645 12.614 1.00 37.88 42 O SER A 341 27.737 62.076 11.544 1.00 42.10 43 CB SER A 341 29.025 64.627 13.042 1.00 39.34 44 OG SER A 341 29.347 64.792 11.672 1.00 44.58 45 N ARG A 342 26.415 62.868 13.158 1.00 36.98 46 CA ARG A 342 25.187 62.437 12.517 1.00 35.20 47 C ARG A 342 24.853 63.417 11.393 1.00 33.18 48 O ARG A 342 25.508 64.443 11.252 1.00 33.16 49 CB ARC A 342 24.070 62.394 13.566 1.00 38.57 50 CG ARG A 342 24.321 61.381 14.689 1.00 39.10 51 CD ARG A 342 23.191 61.364 15.712 1.00 43.21 52 NE ARG A 342 23.231 62.544 16.570 1.00 45.40 53 CZ ARG A 342 24.086 62.714 17.573 1.00 48.22 54 NE1 ARG A 342 24.977 61.777 17.860 1.00 52.78 55 NH2 ARG A 342 24.059 63.831 18.286 1.00 54.34 56 N PRO A 343 23.843 63.112 10.570 1.00 33.03 57 CA PRO A 343 23.497 64.040 9.481 1.00 34.14 58 C PRO A 343 22.907 65.339 10.035 1.00 34.06 59 O PRO A 343 22.302 65.341 11.106 1.00 35.44 60 CB PRO A 343 22.448 63.266 8.667 1.00 33.07 61 CG PRO A 343 22.700 61.811 9.025 1.00 35.06 62 CD PRO A 343 23.029 61.885 10.499 1.00 33.27 63 N SER A 344 23.080 66.445 9.325 1.00 32.17 64 CA SER A 344 22.490 67.691 9.792 1.00 31.75 65 C SER A 344 21.014 67.617 9.414 1.00 32.07 66 O SER A 344 20.660 67.115 8.344 1.00 30.21 67 CB SER A 344 23.144 68.907 9.118 1.00 32.20 68 OG SER A 344 22.665 69.113 7.799 1.00 32.50 69 N PRO A 345 20.127 68.088 10.300 1.00 32.31 70 CA PRO A 345 18.701 68.039 9.975 1.00 30.84 71 C PRO A 345 18.381 68.710 8.629 1.00 29.64 72 O PRO A 345 17.506 68.256 7.891 1.00 30.14 73 CB PRO A 345 18.055 68.741 11.174 1.00 30.96 74 CG PRO A 345 18.941 68.301 12.307 1.00 33.18 75 CD PRO A 345 20.339 68.457 11.713 1.00 33.65 76 N PHE A 346 19.103 69.769 8.292 1.00 28.34 77 CA PHE A 346 18.844 70.447 7.034 1.00 31.46 78 C PHE A 346 19.085 69.522 5.831 1.00 32.46 79 O PHE A 346 18.269 69.465 4.907 1.00 32.59 80 CB PHE A 346 19.711 71.706 6.916 1.00 32.72 81 CG PHE A 346 19.613 72.382 5.579 1.00 36.34 82 CD1 PHE A 346 18.430 72.981 5.172 1.00 40.58 83 CD2 PHE A 346 20.702 72.411 4.722 1.00 36.76 84 CE1 PHE A 346 18.333 73.609 3.933 1.00 38.98 85 CE2 PHE A 346 20.615 73.037 3.482 1.00 40.15 86 CZ PHE A 346 19.425 73.637 3.086 1.00 38.60 87 N ASP A 347 20.203 68.797 5.850 1.00 32.92 88 CA ASP A 347 20.534 67.877 4.764 1.00 33.58 89 C ASP A 347 19.555 66.704 4.733 1.00 34.26 90 O ASP A 347 19.192 66.212 3.666 1.00 32.29 91 CB ASP A 347 21.967 67.349 4.921 1.00 28.72 92 CG ASP A 347 23.008 68.364 4.521 1.00 39.62 93 OD1 ASP A 347 24.225 68.085 4.671 1.00 42.08 94 OD2 ASP A 347 22.609 69.449 4.046 1.00 46.23 95 N LEU A 348 19.120 66.276 5.911 1.00 34.31 96 CA LEU A 348 18.197 65.159 6.036 1.00 37.70 97 C LEU A 348 16.742 65.441 5.629 1.00 38.98 98 O LEU A 348 16.137 64.651 4.902 1.00 38.11 99 CB LEU A 348 18.220 64.641 7.482 1.00 40.66 100 CG LEU A 348 17.333 63.441 7.840 1.00 41.99 101 CO1 LEU A 348 17.738 62.212 7.005 1.00 42.77 102 CD2 LEU A 348 17.476 63.131 9.341 1.00 41.00 103 N PHE A 349 16.183 66.560 6.083 1.00 39.68 104 CA PHE A 349 14.781 66.875 5.794 1.00 42.09 105 C PHE A 349 14.466 67.883 4.695 1.00 45.09 106 O PHE A 349 13.431 67.779 4.038 1.00 48.27 107 CB PHE A 349 14.074 67.328 7.071 1.00 37.36 108 CG PHE A 349 14.189 66.356 8.200 1.00 36.93 109 CD1 PHE A 349 15.021 66.624 9.282 1.00 38.16 110 CD2 PHE A 349 13.487 65.156 8.174 1.00 38.04 111 CE1 PHE A 349 15.155 65.715 10.319 1.00 38.11 112 CE2 PHE A 349 13.614 64.231 9.213 1.00 37.58 113 CZ PHE A 349 14.449 64.511 10.283 1.00 40.39 114 N ILE A 350 15.323 68.874 4.500 1.00 46.66 115 CA ILE A 350 15.052 69.854 3.461 1.00 48.94 116 C ILE A 350 15.695 69.400 2.150 1.00 51.15 117 O ILE A 350 15.007 69.095 1.179 1.00 50.51 118 CB ILE A 350 15.592 71.241 3.860 1.00 48.52 119 CG1 ILE A 350 15.172 71.562 5.299 1.00 49.25 120 CG2 ILE A 350 15.052 72.300 2.923 1.00 49.68 121 CD1 ILE A 350 13.689 71.358 5.567 1.00 46.80 122 N ARG A 351 17.021 69.335 2.155 1.00 52.64 123 CA ARG A 351 17.807 68.931 1.000 1.00 53.76 124 C ARG A 351 17.510 67.486 0.581 1.00 53.61 125 O ARG A 351 17.506 67.164 0.603 1.00 53.55 126 CB ARG A 351 19.287 69.095 1.341 1.00 56.64 127 CG ARG A 351 20.166 69.584 0.206 1.00 62.18 128 CD ARG A 351 21.225 70.527 0.752 1.00 66.96 129 NE ARG A 351 22.389 70.642 0.119 1.00 71.13 130 CZ ARG A 351 23.229 69.643 0.370 1.00 76.72 131 NH1 ARG A 351 23.027 68.455 0.184 1.00 78.73 132 NH2 ARG A 351 24.275 69.829 1.168 1.00 77.63 133 N LYS A 352 17.253 66.626 1.560 1.00 53.86 134 CA LYS A 352 16.954 65.215 1.312 1.00 54.12 135 C LYS A 352 18.151 64.428 0.772 1.00 52.02 136 O LYS A 352 17.996 63.522 0.046 1.00 51.77 137 CB LYS A 352 15.775 65.075 0.347 1.00 57.77 138 CG LYS A 352 14.476 65.689 0.846 1.00 62.15 139 CD LYS A 352 13.348 65.439 0.154 1.00 71.06 140 CE LYS A 352 12.098 66.249 0.171 1.00 74.25 141 NZ LYS A 352 12.293 67.707 0.085 1.00 78.35 142 N SER A 353 19.342 64.789 1.233 1.00 48.01 143 CA SER A 353 20.568 64.112 0.832 1.00 45.29 144 C SER A 353 21.544 64.154 2.016 1.00 40.67 145 O SER A 353 22.546 64.875 1.994 1.00 40.76 146 CB SER A 353 21.177 64.791 0.398 1.00 47.97 147 CG SER A 353 21.448 66.155 0.147 1.00 56.20 148 N PRO A 354 21.244 63.375 3.070 1.00 36.53 149 CA PRO A 354 22.004 63.239 4.319 1.00 32.68 150 C PRO A 354 23.399 62.660 4.139 1.00 31.88 151 O PRO A 354 23.615 61.787 3.302 1.00 29.76 152 CB PRO A 354 21.147 62.294 5.160 1.00 30.29 153 CG PRO A 354 19.799 62.340 4.513 1.00 41.68 154 CD PRO A 354 20.106 62.445 3.065 1.00 33.29 155 N THR A 355 24.342 63.154 4.932 1.00 30.03 156 CA THR A 355 25.704 62.644 4.902 1.00 29.70 157 C THR A 355 26.236 62.578 6.326 1.00 30.82 158 O THR A 355 25.773 63.298 7.213 1.00 30.67 159 CB THR A 355 26.669 63.558 4.136 1.00 32.14 160 OC1 THR A 355 26.806 64.785 4.860 1.00 29.97 161 CG2 THR A 355 26.175 63.837 2.707 1.00 31.76 162 N ILE A 356 27.195 61.693 6.558 1.00 30.53 163 CA ILE A 356 27.816 61.631 7.868 1.00 31.56 164 C ILE A 356 29.279 61.860 7.575 1.00 31.79 165 O ILE A 356 29.752 61.561 6.475 1.00 30.35 166 CB ILE A 356 27.584 60.285 8.583 1.00 30.05 167 CG1 ILE A 356 28.101 59.133 7.729 1.00 31.32 168 CG2 ILE A 356 26.092 60.131 8.890 1.00 31.27 169 CD1 ILE A 356 27.843 57.772 8.337 1.00 36.89 170 N THR A 357 29.995 62.402 8.550 1.00 33.31 171 CA THR A 357 31.395 62.719 8.349 1.00 33.68 172 C THR A 357 32.282 62.197 9.456 1.00 35.47 173 O THR A 357 31.993 62.372 10.641 1.00 36.65 174 CB THE A 357 31.589 64.265 8.245 1.00 33.81 175 OG1 THR A 357 30.917 64.756 7.077 1.00 33.71 176 CG2 THR A 357 33.065 64.632 8.179 1.00 29.63 177 N CYS A 358 33.372 61.566 9.052 1.00 35.41 178 CA CYS A 358 34.346 61.039 9.990 1.00 38.12 179 C CYS A 358 35.507 62.030 9.935 1.00 37.77 180 O CYS A 358 36.127 62.205 8.890 1.00 36.67 181 CB CYS A 358 34.811 59.655 9.532 1.00 40.37 182 SG CYS A 358 35.831 58.729 10.726 1.00 49.83 183 N LEU A 359 35.778 62.691 11.054 1.00 39.77 184 CA LEU A 359 36.853 63.668 11.127 1.00 42.86 185 C LEU A 359 38.007 63.168 11.977 1.00 46.01 186 O LEU A 359 37.831 62.852 13.152 1.00 47.43 187 CB LEU A 359 36.335 64.988 11.711 1.00 42.74 188 CG LEU A 359 37.392 65.996 12.196 1.00 45.03 189 CD1 LEU A 359 38.262 66.448 11.043 1.00 47.59 190 CD2 LEU A 359 36.711 67.197 12.838 1.00 47.51 191 N VAL A 360 39.189 63.107 11.379 1.00 48.26 192 CA VAL A 360 40.380 62.669 12.090 1.00 52.34 193 C VAL A 360 41.357 63.835 12.217 1.00 55.48 194 O VAL A 360 41.672 64.508 11.234 1.00 55.57 195 CB VAL A 360 41.073 61.500 11.353 1.00 53.36 196 CG1 VAL A 360 42.360 61.119 12.071 1.00 51.62 197 CG2 VAL A 360 40.133 60.301 11.284 1.00 51.77 198 N VAL A 361 41.827 64.080 13.435 1.00 58.92 199 CA VAL A 361 42.766 65.167 13.684 1.00 63.13 200 C VAL A 361 44.094 64.607 14.174 1.00 67.77 201 O VAL A 361 44.134 63.862 15.154 1.00 68.38 202 CB VAL A 361 42.223 66.158 14.747 1.00 60.50 203 CG1 VAL A 361 43.245 67.242 15.014 1.00 56.92 204 CG2 VAL A 361 40.929 66.786 14.270 1.00 56.10 205 N ASP A 362 45.174 64.965 13.485 1.00 72.90 206 CA ASP A 362 46.515 64.502 13.841 1.00 78.30 207 C ASP A 362 47.356 65.696 14.284 1.00 81.68 208 O ASP A 362 47.891 66.432 13.452 1.00 81.72 209 CB ASP A 362 47.185 63.829 12.638 1.00 80.22 210 CG ASP A 362 48.444 63.070 13.020 1.00 84.67 211 OD1 ASP A 362 49.122 63.487 13.983 1.00 87.54 212 OD2 ASP A 362 48.763 62.063 12.351 1.00 87.19 213 N LEU A 363 47.474 65.877 15.597 1.00 85.84 214 CA LEU A 363 48.234 66.986 16.165 1.00 89.95 215 C LEU A 363 49.677 67.038 15.672 1.00 92.20 216 O LEU A 363 50.214 68.117 15.432 1.00 92.55 217 CB LEU A 363 48.210 66.906 17.691 1.00 91.66 218 CG LEU A 363 46.823 66.881 18.342 1.00 92.93 219 CD1 LEU A 363 46.976 66.787 19.854 1.00 95.41 220 CD2 LEU A 363 46.049 68.129 17.963 1.00 92.73 221 N ALA A 364 50.304 65.874 15.527 1.00 94.76 222 CA ALA A 364 51.684 65.799 15.049 1.00 97.66 223 C ALA A 364 51.769 64.206 13.890 1.00 99.72 224 O ALA A 364 51.604 63.602 14.079 1.00 100.44 225 CB ALA A 364 52.604 65.365 16.179 1.00 97.99 226 N PRO A 365 52.023 65.303 12.671 1.00 101.15 227 CA PRO A 365 52.116 64.427 11.498 1.00 102.25 228 C PRO A 365 53.437 63.705 11.245 1.00 103.43 229 O PRO A 365 54.497 64.326 11.166 1.00 104.19 230 CB PRO A 365 51.771 65.363 10.339 1.00 101.91 231 CG PRO A 365 50.983 66.479 11.002 1.00 102.27 232 CD PRO A 365 51.767 66.690 12.254 1.00 101.40 233 N SER A 366 53.344 62.385 11.121 1.00 104.18 234 CA SER A 366 54.468 61.512 10.801 1.00 104.43 235 C SER A 366 53.924 61.027 9.463 1.00 104.05 236 O SER A 366 52.736 60.712 9.373 1.00 104.36 237 CB SER A 366 54.545 60.351 11.788 1.00 105.50 238 OG SER A 366 53.377 59.560 11.687 1.00 106.70 239 N LYS A 367 54.739 60.955 8.418 1.00 103.19 240 CA LYS A 367 54.138 60.559 7.156 1.00 102.08 241 C LYS A 367 53.970 59.109 6.733 1.00 100.74 242 O LYS A 367 54.917 58.366 6.460 1.00 101.05 243 CB LYS A 367 54.732 61.364 5.998 1.00 103.30 244 CO LYS A 367 56.216 61.257 5.755 1.00 105.00 245 CD LYS A 367 56.554 62.226 4.633 1.00 104.80 246 CE LYS A 367 57.990 62.133 4.170 1.00 104.70 247 NZ LYS A 367 58.214 63.076 3.034 1.00 105.18 248 N GLY A 368 52.691 58.761 6.678 1.00 98.70 249 CA GLY A 368 52.192 57.464 6.272 1.00 95.62 250 C GLY A 368 50.799 57.900 5.856 1.00 93.12 251 O GLY A 368 50.457 59.062 6.065 1.00 93.17 252 N THR A 369 49.983 57.031 5.277 1.00 90.15 253 CA THR A 369 48.652 57.475 4.880 1.00 86.41 254 C THR A 369 47.623 57.180 5.964 1.00 83.04 255 O THR A 369 47.746 56.198 6.699 1.00 82.54 256 CB THR A 369 48.203 56.808 3.559 1.00 87.73 257 OG1 THR A 369 48.178 55.383 3.721 1.00 88.60 258 CG2 THR A 369 49.157 57.177 2.429 1.00 86.64 259 N VAL A 370 46.620 58.048 6.073 1.00 79.07 260 CA VAL A 370 45.559 57.871 7.058 1.00 74.46 261 C VAL A 370 44.339 57.325 6.332 1.00 72.21 262 O VAL A 370 43.762 57.998 5.482 1.00 71.35 263 CB VAL A 370 45.180 59.199 7.732 1.00 73.33 264 CG1 VAL A 370 44.254 58.933 8.904 1.00 70.92 265 CG2 VAL A 370 46.427 59.926 8.185 1.00 69.77 266 N ASN A 371 43.947 56.102 6.674 1.00 70.13 267 CA ASN A 371 42.809 55.463 6.027 1.00 68.15 268 C ASN A 371 41.521 55.443 6.838 1.00 65.65 269 O ASN A 371 41.533 55.248 8.054 1.00 64.64 270 CB ASN A 371 43.179 54.036 5.631 1.00 70.12 271 CG ASN A 371 44.270 53.995 4.592 1.00 73.56 272 OD1 ASN A 371 44.081 54.447 3.462 1.00 75.10 273 ND2 ASN A 371 45.427 53.463 4.969 1.00 74.76 274 N LEU A 372 40.408 55.651 6.141 1.00 62.66 275 CA LEU A 372 39.088 55.641 6.754 1.00 59.53 276 C LEU A 372 38.226 54.673 5.963 1.00 56.68 277 O LEU A 372 38.071 54.812 4.753 1.00 56.70 278 CB LEU A 372 38.459 57.040 6.728 1.00 59.44 279 CG LEU A 372 39.217 58.172 7.422 1.00 60.55 280 CD1 LEU A 372 38.323 59.386 7.521 1.00 61.28 281 CD2 LEU A 372 39.644 57.739 8.807 1.00 62.83 282 N THR A 373 37.669 53.689 6.654 1.00 53.76 283 CA THR A 373 36.834 52.685 6.015 1.00 51.64 284 C THR A 373 35.420 52.750 6.588 1.00 48.20 285 O THR A 373 35.245 52.799 7.804 1.00 46.65 286 CB THR A 373 37.399 51.275 6.268 1.00 53.15 287 OG1 THR A 373 38.811 51.276 6.027 1.00 57.77 288 CG2 THR A 373 36.729 50.261 5.353 1.00 53.75 289 N TRP A 374 34.419 52.749 5.715 1.00 45.34 290 CA TRP A 374 33.025 52.801 6.158 1.00 44.94 291 C TRP A 374 32.341 51.439 6.059 1.00 43.68 292 O TRP A 374 32.636 50.655 5.162 1.00 42.67 293 CD TRP A 374 32.209 53.795 5.316 1.00 41.63 294 CG TRP A 374 32.623 55.229 5.443 1.00 41.50 295 CD1 TRP A 374 33.476 55.912 4.623 1.00 39.67 296 CD2 TRP A 374 32.205 56.159 6.452 1.00 35.69 297 NE1 TRP A 374 33.612 57.208 5.059 1.00 35.06 298 CE2 TRP A 374 32.844 57.386 6.178 1.00 34.53 299 CE3 TRP A 374 31.353 56.072 7.558 1.00 32.37 300 CZ2 TRP A 374 32.657 58.521 6.971 1.00 35.43 301 CZ3 TRP A 374 31.166 57.199 8.349 1.00 36.11 302 CH2 TRP A 374 31.818 58.410 8.050 1.00 37.51 303 N SER A 375 31.421 51.170 6.981 1.00 43.53 304 CA SER A 375 30.666 49.922 6.960 1.00 43.57 305 C SER A 375 29.330 50.089 7.662 1.00 42.59 306 O SER A 375 29.189 50.931 8.550 1.00 43.68 307 CD SER A 375 31.447 48.780 7.626 1.00 45.03 308 OG SER A 375 31.482 48.909 9.034 1.00 45.66 309 N ARG A 376 28.349 49.301 7.234 1.00 40.79 310 CA ARG A 376 27.031 49.321 7.834 1.00 40.12 311 C ARG A 376 26.911 48.102 8.749 1.00 40.59 312 O ARG A 376 27.207 46.982 8.348 1.00 40.90 313 CB ARG A 376 25.947 49.255 6.766 1.00 40.03 314 CG ARG A 376 25.855 50.468 5.863 1.00 43.20 315 CD ARG A 376 24.402 50.717 5.501 1.00 41.05 316 NE ARG A 376 24.120 50.429 4.108 1.00 50.71 317 CZ ARG A 376 22.895 50.300 3.612 1.00 53.97 318 NH1 ARG A 376 21.842 50.428 4.407 1.00 51.88 319 NH2 ARG A 376 22.726 50.058 2.318 1.00 55.55 320 N ALA A 377 26.471 48.319 9.978 1.00 40.20 321 CA ALA A 377 26.327 47.218 10.919 1.00 40.25 322 C ALA A 377 25.470 46.100 10.314 1.00 40.38 323 O ALA A 377 25.621 44.943 10.678 1.00 41.16 324 CD ALA A 377 25.697 47.721 12.222 1.00 33.12 325 N SER A 378 24.585 46.456 9.386 1.00 40.21 326 CA SER A 378 23.697 45.491 8.746 1.00 41.95 327 C SER A 378 24.412 44.694 7.664 1.00 44.92 328 O SER A 378 23.856 43.734 7.134 1.00 44.28 329 CD SER A 378 22.504 46.199 8.108 1.00 40.91 330 OG SER A 378 22.907 46.863 6.920 1.00 40.09 331 N GLY A 379 25.633 45.107 7.332 1.00 46.93 332 CA GLY A 379 26.405 44.419 6.313 1.00 49.77 333 C GLY A 379 26.088 44.884 4.904 1.00 50.60 334 O GLY A 379 26.817 44.576 3.958 1.00 52.95 335 N LYS A 380 24.995 45.626 4.755 1.00 53.72 336 CA LYS A 380 24.612 46.122 3.443 1.00 54.13 337 C LYS A 380 25.689 47.036 2.845 1.00 48.16 338 O LYS A 380 26.592 47.513 3.544 1.00 45.65 339 CD LYS A 380 23.262 46.848 3.517 1.00 62.44 340 CG LYS A 380 22.078 45.908 3.710 1.00 67.72 341 CD LYS A 380 20.748 46.625 3.550 1.00 69.32 342 CE LYS A 380 19.587 45.644 3.619 1.00 73.14 343 NZ LYS A 380 18.267 46.320 3.467 1.00 77.37 344 N PRO A 381 25.614 47.277 1.529 1.00 56.07 345 CA PRO A 381 26.586 48.128 0.835 1.00 56.46 346 C PRO A 381 26.535 49.607 1.225 1.00 54.32 347 O PRO A 381 25.467 50.154 1.511 1.00 56.76 348 CB PRO A 381 26.225 47.936 0.640 1.00 60.70 349 CG PRO A 381 25.481 46.622 0.667 1.00 62.01 350 CD PRO A 381 24.655 46.695 0.574 1.00 59.24 351 N VAL A 382 27.701 50.244 1.234 1.00 55.74 352 CA VAL A 382 27.795 51.669 1.531 1.00 55.58 353 C VAL A 382 28.192 52.353 0.220 1.00 55.56 354 O VAL A 382 28.866 51.752 0.620 1.00 55.22 355 CE VAL A 382 28.874 51.980 2.607 1.00 55.39 356 CG1 VAL A 382 28.592 51.196 3.878 1.00 55.94 357 CG2 VAL A 382 30.261 51.664 2.075 1.00 53.06 358 N ASN A 383 27.773 53.600 0.045 1.00 54.38 359 CA ASN A 383 28.090 54.354 1.164 1.00 54.63 360 C ASN A 383 29.532 54.843 1.190 1.00 53.85 361 O ASN A 383 30.303 54.630 0.254 1.00 52.58 362 CB ASN A 383 27.171 55.566 1.282 1.00 59.07 363 CG ASN A 383 25.717 55.186 1.356 1.00 64.60 364 OD1 ASN A 383 24.836 56.024 1.169 1.00 70.14 365 ND2 ASN A 383 25.450 53.915 1.638 1.00 71.07 366 N HIS A 384 29.890 55.506 2.281 1.00 53.46 367 CA HIS A 384 31.229 56.057 2.426 1.00 52.22 368 C HIS A 384 31.326 57.302 1.540 1.00 49.10 369 O HIS A 384 30.400 58.105 1.485 1.00 45.53 370 CE HIS A 384 31.489 56.417 3.893 1.00 59.11 371 CG HIS A 384 31.676 55.223 4.778 1.00 62.16 372 ND1 HIS A 384 32.738 54.357 4.639 1.00 69.15 373 CD2 HIS A 384 30.931 54.745 5.803 1.00 70.28 374 CE1 HIS A 384 32.640 53.394 5.539 1.00 75.01 375 NE2 HIS A 384 31.553 53.605 6.258 1.00 74.58 376 N SER A 385 32.448 57.454 0.849 1.00 45.07 377 CA SER A 385 32.641 58.583 0.040 1.00 44.61 378 C SER A 385 33.617 59.627 0.504 1.00 44.58 379 O SER A 385 34.380 59.356 1.421 1.00 44.21 380 CB SER A 385 33.113 58.076 1.409 1.00 44.61 381 OG SER A 385 34.293 57.290 1.311 1.00 41.13 382 N THR A 386 33.575 60.827 0.065 1.00 44.32 383 CA THR A 386 34.450 61.916 0.346 1.00 44.35 384 C THR A 386 35.487 62.156 0.737 1.00 44.09 385 O THR A 386 35.149 62.326 1.911 1.00 44.06 386 CE THR A 386 33.664 63.226 0.580 1.00 45.20 387 OG1 THR A 386 32.744 63.045 1.662 1.00 51.89 388 CG2 THR A 386 34.616 64.368 0.936 1.00 47.20 389 N ARG A 387 36.749 62.176 0.326 1.00 44.39 390 CA ARG A 387 37.870 62.378 1.233 1.00 46.68 391 C ARG A 387 38.520 63.763 1.070 1.00 47.05 392 O ARG A 387 38.750 64.228 0.049 1.00 46.65 393 CE ARG A 387 38.906 61.284 0.979 1.00 48.13 394 CG ARG A 387 40.112 61.330 1.890 1.00 52.77 395 CD ARG A 387 41.247 60.494 1.320 1.00 56.60 396 NE ARG A 387 42.459 60.622 2.121 1.00 60.65 397 CZ ARG A 387 42.705 59.917 3.218 1.00 61.97 398 NH1 ARG A 387 41.821 59.022 3.636 1.00 64.45 399 NH2 ARG A 387 43.819 60.131 3.911 1.00 60.54 400 N LYS A 388 38.820 64.415 2.190 1.00 46.93 401 CA LYS A 388 39.457 65.730 2.167 1.00 47.51 402 C LYS A 388 40.630 65.777 3.143 1.00 48.33 403 O LYS A 388 40.493 65.401 4.306 1.00 46.08 404 CB LYS A 388 38.452 66.823 2.537 1.00 46.64 405 CG LYS A 388 37.274 66.909 1.603 1.00 52.75 406 CD LYS A 388 36.154 67.739 2.195 1.00 58.62 407 CE LYS A 388 34.863 67.538 1.418 1.00 62.49 408 NZ LYS A 388 33.719 68.204 2.101 1.00 67.33 409 N GLU A 389 41.780 66.236 2.651 1.00 50.07 410 CA GLU A 389 42.998 66.357 3.454 1.00 51.86 411 C GLU A 389 43.474 67.807 3.462 1.00 52.81 412 O GLU A 389 43.683 68.408 2.405 1.00 49.21 413 CB GLU A 389 44.106 65.474 2.877 1.00 54.67 414 CG GLU A 389 43.890 63.984 3.056 1.00 65.65 415 CD GLU A 389 44.992 63.159 2.412 1.00 72.66 416 OE1 GLU A 389 46.182 63.449 2.671 1.00 75.92 417 OE2 GLU A 389 44.669 62.220 1.650 1.00 75.78 418 N GLU A 390 43.652 68.371 4.651 1.00 56.06 419 CA GLU A 390 44.100 69.751 4.754 1.00 61.17 420 C GLU A 390 45.146 69.971 5.835 1.00 64.70 421 O GLU A 390 45.002 69.528 6.977 1.00 64.01 422 CB GLU A 390 42.908 70.673 4.993 1.00 64.35 423 CG GLU A 390 43.283 72.121 5.233 1.00 74.80 424 CD GLU A 390 42.091 73.052 5.121 1.00 85.97 425 OE1 GLU A 390 41.053 72.778 5.764 1.00 92.60 426 OE2 GLU A 390 42.197 74.059 4.388 1.00 92.18 427 N LYS A 391 46.204 70.679 5.461 1.00 68.18 428 CA LYS A 391 47.288 70.960 6.388 1.00 71.58 429 C LYS A 391 47.298 72.385 6.920 1.00 76.11 430 O LYS A 391 46.927 73.335 6.231 1.00 75.89 431 CB LYS A 391 48.627 70.654 5.728 1.00 67.28 432 N GLN A 392 47.724 72.508 8.168 1.00 81.85 433 CA GLN A 392 47.854 73.786 8.846 1.00 88.38 434 C GLN A 392 49.118 73.574 9.657 1.00 92.30 435 O GLN A 392 49.100 72.848 10.648 1.00 93.25 436 CB GLN A 392 46.662 74.045 9.777 1.00 85.87 437 CG GLN A 392 45.752 75.178 9.318 1.00 90.76 438 CD GLN A 392 44.727 75.573 10.369 1.00 93.39 439 OE1 GLN A 392 45.076 75.913 11.502 1.00 92.93 440 NE2 GLN A 392 43.453 75.538 9.993 1.00 93.97 441 N ARG A 393 50.221 74.174 9.220 1.00 96.24 442 CA ARG A 393 51.492 74.011 9.916 1.00 100.53 443 C ARG A 393 51.412 74.350 11.403 1.00 102.30 444 O ARG A 393 52.422 74.327 12.107 1.00 101.15 445 CB ARG A 393 52.579 74.853 9.245 1.00 106.99 446 CG ARG A 393 52.404 76.349 9.396 1.00 109.77 447 CD ARG A 393 53.493 77.079 8.636 1.00 115.73 448 NE ARG A 393 53.515 78.505 8.935 1.00 119.73 449 CZ ARG A 393 54.333 79.373 8.350 1.00 121.60 450 NH1 ARG A 393 55.194 78.955 7.430 1.00 121.59 451 NH2 ARG A 393 54.292 80.655 8.684 1.00 121.49 452 N ASN A 394 50.209 74.658 11.876 1.00 103.98 453 CA ASN A 394 50.005 74.970 13.281 1.00 106.60 454 C ASN A 394 50.275 73.682 14.051 1.00 106.89 455 O ASN A 394 51.084 73.650 14.978 1.00 108.55 456 CB ASN A 394 48.564 75.427 13.520 1.00 108.97 457 CG ASN A 394 48.326 75.891 14.947 1.00 112.83 458 OD1 ASN A 394 47.190 76.141 15.348 1.00 114.53 459 ND2 ASN A 394 49.402 76.016 15.719 1.00 114.40 460 N GLY A 395 49.593 72.616 13.648 1.00 105.53 461 CA GLY A 395 49.771 71.331 14.298 1.00 101.15 462 C GLY A 395 48.585 70.423 14.050 1.00 97.82 463 O GLY A 395 48.125 69.721 14.952 1.00 99.41 464 N THR A 396 48.084 70.423 12.822 1.00 94.50 465 CA THR A 396 46.937 69.589 12.522 1.00 89.02 466 C THR A 396 46.763 69.174 11.071 1.00 83.93 467 O THR A 396 46.477 70.000 10.204 1.00 83.27 468 CB THR A 396 45.625 70.278 12.970 1.00 92.03 469 OG1 THR A 396 45.648 70.484 14.388 1.00 94.17 470 CG2 THR A 396 44.414 69.421 12.596 1.00 95.48 471 N LEU A 397 46.942 67.882 10.821 1.00 79.69 472 CA LEU A 397 46.729 67.320 9.500 1.00 74.75 473 C LEU A 397 45.295 66.827 9.604 1.00 71.50 474 O LEU A 397 45.052 65.720 10.081 1.00 74.81 475 CB LEU A 397 47.640 66.120 9.240 1.00 75.72 476 CG LEU A 397 47.188 65.250 8.053 1.00 70.67 477 CD1 LEU A 397 47.668 65.858 6.738 1.00 69.05 478 CD2 LEU A 397 47.723 63.832 8.213 1.00 72.96 479 N THR A 398 44.348 67.659 9.195 1.00 67.61 480 CA THR A 398 42.945 67.286 9.252 1.00 61.30 481 C THR A 398 42.559 66.393 8.076 1.00 56.61 482 O THR A 398 42.960 66.626 6.934 1.00 54.95 483 CB THR A 398 42.044 68.530 9.248 1.00 61.75 484 OG1 THR A 398 42.225 69.255 10.471 1.00 65.40 485 CG2 THR A 398 40.584 68.129 9.108 1.00 63.39 486 N VAL A 399 41.783 65.359 8.371 1.00 51.84 487 CA VAL A 399 41.321 64.437 7.349 1.00 48.05 488 C VAL A 399 39.870 64.085 7.610 1.00 44.81 489 O VAL A 399 39.502 63.689 8.719 1.00 44.41 490 CB VAL A 399 42.132 63.134 7.349 1.00 49.35 491 CG1 VAL A 399 41.590 62.191 6.295 1.00 49.43 492 CG2 VAL A 399 43.594 63.432 7.090 1.00 53.10 493 N THR A 400 39.036 64.246 6.596 1.00 42.44 494 CA THR A 400 37.635 63.909 6.757 1.00 40.44 495 C THR A 400 37.151 63.068 5.602 1.00 38.07 496 O THR A 400 37.692 63.117 4.498 1.00 36.13 497 CB THR A 400 36.731 65.152 6.834 1.00 39.64 498 OG1 THR A 400 36.638 65.755 5.539 1.00 43.72 499 CG2 THR A 400 37.278 66.158 7.822 1.00 38.32 500 N SER A 401 36.140 62.265 5.884 1.00 36.90 501 CA SER A 401 35.531 61.432 4.876 1.00 35.46 502 C SER A 401 34.043 61.612 5.084 1.00 33.95 503 O SER A 401 33.538 61.447 6.192 1.00 34.80 504 CB SER A 401 35.906 59.962 5.060 1.00 36.91 505 OG SER A 401 35.299 59.183 4.040 1.00 40.84 506 N THR A 402 33.352 61.965 4.014 1.00 32.28 507 CA THR A 402 31.928 62.178 4.068 1.00 31.85 508 C THR A 402 31.245 61.092 3.264 1.00 31.76 509 O THR A 402 31.554 60.863 2.090 1.00 30.55 510 CB THR A 402 31.570 63.549 3.505 1.00 31.33 511 OG1 THR A 402 32.284 64.542 4.238 1.00 32.83 512 CG2 THR A 402 30.078 63.818 3.632 1.00 32.70 513 N LEU A 403 30.299 60.433 3.912 1.00 30.72 514 CA LEU A 403 29.582 59.343 3.300 1.00 30.33 515 C LEU A 403 28.115 59.673 3.097 1.00 29.66 516 O LEU A 403 27.415 59.992 4.052 1.00 28.06 517 CB LEU A 403 29.698 58.098 4.187 1.00 28.34 518 CG LEU A 403 28.968 56.831 3.719 1.00 32.10 519 CG1 LEU A 403 29.777 56.175 2.597 1.00 31.94 520 CD2 LEU A 403 28.810 55.844 4.876 1.00 30.42 521 N PRO A 404 27.638 59.617 1.841 1.00 31.48 522 CA PRO A 404 26.233 59.896 1.534 1.00 33.20 523 C PRO A 404 25.451 58.759 2.194 1.00 34.02 524 O PRO A 404 25.845 57.601 2.104 1.00 32.25 525 CB PRO A 404 26.183 59.812 0.010 1.00 33.28 526 CG PRO A 404 27.590 60.165 0.400 1.00 31.82 527 CD PRO A 404 28.413 59.414 0.603 1.00 31.26 528 N VAL A 405 24.362 59.097 2.865 1.00 34.94 529 CA VAL A 405 23.556 58.117 3.564 1.00 38.63 530 C VAL A 405 22.128 58.059 3.032 1.00 40.02 531 O VAL A 405 21.573 59.063 2.598 1.00 40.31 532 CB VAL A 405 23.548 58.457 5.082 1.00 42.09 533 CG1 VAL A 405 22.128 58.490 5.632 1.00 43.95 534 CG2 VAL A 405 24.405 57.456 5.827 1.00 41.76 535 N GLY A 406 21.536 56.872 3.061 1.00 42.35 536 CA GLY A 406 20.168 56.741 2.597 1.00 43.35 537 C GLY A 406 19.246 57.422 3.587 1.00 43.87 538 O GLY A 406 19.446 57.314 4.797 1.00 42.68 539 N THR A 407 18.248 58.134 3.077 1.00 44.40 540 CA THR A 407 17.294 58.840 3.923 1.00 47.37 541 C THR A 407 16.473 57.887 4.778 1.00 48.27 542 O THR A 407 16.392 58.051 5.993 1.00 48.77 543 CE THR A 407 16.312 59.678 3.078 1.00 48.44 544 OG1 THR A 407 17.001 60.791 2.504 1.00 50.00 545 CG2 THR A 407 15.164 60.187 3.938 1.00 53.23 546 N ARG A 408 15.854 56.903 4.130 1.00 48.10 547 CA ARG A 408 15.021 55.935 4.821 1.00 48.54 548 C ARG A 408 15.827 55.060 5.765 1.00 48.48 549 O ARG A 408 15.418 54.831 6.903 1.00 47.34 550 CE ARG A 408 14.275 55.070 3.810 1.00 50.16 551 N ASP A 409 16.966 54.567 5.294 1.00 48.72 552 CA ASP A 409 17.813 53.714 6.121 1.00 50.88 553 C ASP A 409 18.179 54.413 7.426 1.00 49.92 554 O ASP A 409 18.132 53.811 8.502 1.00 49.76 555 CE ASP A 409 19.088 53.340 5.362 1.00 56.18 556 CG ASP A 409 18.799 52.587 4.074 1.00 64.80 557 OD1 ASP A 409 18.118 51.538 4.144 1.00 71.41 558 OD2 ASP A 409 19.247 53.039 2.995 1.00 68.29 559 N TRP A 410 18.533 55.692 7.327 1.00 48.36 560 CA TRP A 410 18.914 56.458 8.503 1.00 46.32 561 C TRP A 410 17.736 56.647 9.447 1.00 46.21 562 O TRP A 410 17.869 56.489 10.660 1.00 44.64 563 CE TRP A 410 19.480 57.826 8.108 1.00 42.82 564 CG TRP A 410 19.890 58.599 9.304 1.00 39.31 565 CD1 TRP A 410 19.133 59.496 9.997 1.00 37.29 566 CD2 TRP A 410 21.093 58.419 10.057 1.00 35.49 567 NE1 TRP A 410 19.781 59.874 11.143 1.00 39.24 568 CE2 TRP A 410 20.987 59.228 11.205 1.00 32.76 569 CE3 TRP A 410 22.249 57.644 9.872 1.00 32.07 570 CZ2 TRP A 410 21.994 59.291 12.176 1.00 29.59 571 CZ3 TRP A 410 23.248 57.704 10.831 1.00 33.68 572 CH2 TRP A 410 23.111 58.527 11.975 1.00 30.56 573 N ILE A 411 16.584 56.989 8.888 1.00 48.11 574 CA ILE A 411 15.391 57.192 9.699 1.00 50.90 575 C ILE A 411 14.951 55.888 10.358 1.00 52.46 576 O ILE A 411 14.371 55.902 11.442 1.00 53.34 577 CB ILE A 411 14.234 57.755 8.854 1.00 51.58 578 CG1 ILE A 411 14.613 59.144 8.330 1.00 52.81 579 CG2 ILE A 411 12.966 57.828 9.685 1.00 51.95 580 CD1 ILE A 411 13.566 59.777 7.431 1.00 59.38 581 N GLU A 412 15.252 54.763 9.715 1.00 53.21 582 CA GLU A 412 14.872 53.463 10.248 1.00 53.12 583 C GLU A 412 15.853 52.919 11.269 1.00 51.24 584 O GLU A 412 15.610 51.864 11.848 1.00 51.40 585 CB GLU A 412 14.691 52.448 9.119 1.00 59.71 586 CG GLU A 412 13.362 52.578 8.383 1.00 70.52 587 CD GLU A 412 13.201 51.540 7.290 1.00 78.58 588 OE1 GLU A 412 13.402 50.338 7.573 1.00 83.44 589 OE2 GLU A 412 12.868 51.924 6.150 1.00 82.10 590 N GLY A 413 16.966 53.618 11.477 1.00 48.47 591 CA GLY A 413 17.923 53.173 12.474 1.00 44.62 592 C GLY A 413 19.213 52.484 12.068 1.00 44.15 593 O GLY A 413 19.882 51.913 12.927 1.00 43.50 594 N GLU A 414 19.588 52.515 10.793 1.00 42.78 595 CA GLU A 414 20.843 51.878 10.406 1.00 40.78 596 C GLU A 414 21.948 52.495 11.249 1.00 39.97 597 O GLU A 414 21.842 53.645 11.690 1.00 37.43 598 CB GLU A 414 21.155 52.111 8.918 1.00 41.96 599 CG GLU A 414 22.519 51.566 8.441 1.00 44.09 600 CD GLU A 414 22.582 50.036 8.360 1.00 49.01 601 OE1 GLU A 414 23.051 49.387 9.325 1.00 46.84 602 OE2 GLU A 414 22.152 49.479 7.327 1.00 49.89 603 N THR A 415 23.001 51.721 11.485 1.00 39.56 604 CA THR A 415 24.136 52.197 12.253 1.00 40.76 605 C THR A 415 25.369 52.113 11.362 1.00 40.07 606 O THR A 415 25.640 51.067 10.777 1.00 42.10 607 CB THR A 415 24.327 51.362 13.544 1.00 44.69 608 OG1 THR A 415 25.707 51.378 13.929 1.00 51.98 609 CG2 THR A 415 23.856 49.948 13.342 1.00 50.00 610 N TYR A 416 26.100 53.220 11.240 1.00 37.57 611 CA TYR A 416 27.282 53.273 10.386 1.00 34.50 612 C TYR A 416 28.549 53.335 11.201 1.00 36.77 613 O TYR A 416 28.562 53.894 12.300 1.00 35.94 614 CB TYR A 416 27.221 54.484 9.466 1.00 34.15 615 CG TYR A 416 26.003 54.515 8.586 1.00 30.65 616 CD1 TYR A 416 24.744 54.823 9.108 1.00 32.53 617 CD2 TYR A 416 26.101 54.211 7.235 1.00 31.72 618 CE1 TYR A 416 23.616 54.828 8.297 1.00 34.27 619 CE2 TYR A 416 24.981 54.210 6.420 1.00 32.11 620 CZ TYR A 416 23.744 54.520 6.956 1.00 33.86 621 OH TYR A 416 22.636 54.518 6.139 1.00 41.22 622 N GLN A 417 29.624 52.771 10.659 1.00 37.58 623 CA GLN A 417 30.878 52.752 11.386 1.00 39.43 624 C GLN A 417 32.062 53.259 10.582 1.00 39.40 625 O GLN A 417 32.227 52.936 9.406 1.00 39.63 626 CB GLN A 417 31.179 51.331 11.889 1.00 41.37 627 CG GLN A 417 32.386 51.250 12.822 1.00 51.81 628 CD GLN A 417 32.744 49.827 13.214 1.00 61.69 629 OE1 GLN A 417 33.229 49.045 12.390 1.00 67.15 630 NE2 GLN A 417 32.504 49.481 14.479 1.00 63.64 631 N CYS A 418 32.888 54.057 11.236 1.00 39.29 632 CA CYS A 418 34.083 54.581 10.611 1.00 41.80 633 C CYS A 418 35.250 53.880 11.282 1.00 42.50 634 O CYS A 418 35.409 53.954 12.500 1.00 43.33 635 CB CYS A 418 34.208 56.099 10.825 1.00 41.95 636 SG CYS A 418 35.696 56.805 10.043 1.00 54.15 637 N ARG A 419 36.049 53.182 10.491 1.00 43.98 638 CA ARG A 419 37.225 52.497 11.007 1.00 47.51 639 C ARG A 419 38.428 53.323 10.558 1.00 48.11 640 O ARG A 419 38.741 53.381 9.370 1.00 47.85 641 CB ARG A 419 37.289 51.068 10.452 1.00 49.08 642 CG ARG A 419 38.642 50.397 10.586 1.00 54.11 643 CD ARG A 419 38.554 48.892 10.304 1.00 64.71 644 NE ARG A 419 39.868 48.275 10.137 1.00 64.09 645 CZ ARG A 419 40.493 48.163 8.968 1.00 70.31 646 NH1 ARG A 419 39.919 48.619 7.861 1.00 68.32 647 NH2 ARG A 419 41.699 47.608 8.905 1.00 71.53 648 N VAL A 420 39.076 53.990 11.508 1.00 51.04 649 CA VAL A 420 40.231 54.824 11.200 1.00 56.22 650 C VAL A 420 41.532 54.039 11.354 1.00 61.25 651 O VAL A 420 41.780 53.422 12.393 1.00 60.11 652 CB VAL A 420 40.295 56.064 12.115 1.00 54.44 653 CG1 VAL A 420 41.494 56.922 11.729 1.00 52.69 654 CG2 VAL A 420 39.003 56.868 12.005 1.00 55.45 655 N THR A 421 42.359 54.071 10.314 1.00 66.23 656 CA THR A 421 43.631 53.356 10.326 1.00 73.18 657 C THR A 421 44.834 54.266 10.130 1.00 76.87 658 O THR A 421 45.157 54.632 9.000 1.00 77.93 659 CB THR A 421 43.671 52.283 9.225 1.00 73.75 660 OG1 THR A 421 42.628 51.328 9.451 1.00 77.71 661 CG2 THR A 421 45.009 51.567 9.227 1.00 75.35 662 N HIS A 422 45.499 54.624 11.226 1.00 81.02 663 CA HIS A 422 46.678 55.483 11.151 1.00 86.07 664 C HIS A 422 47.914 54.596 11.278 1.00 89.67 665 O HIS A 422 47.947 53.680 12.098 1.00 90.00 666 CB HIS A 422 46.660 56.529 12.269 1.00 87.43 667 CG HIS A 422 47.548 57.708 12.008 1.00 90.73 668 ND1 HIS A 422 47.397 58.524 10.909 1.00 93.83 669 CD2 HIS A 422 48.600 58.204 12.704 1.00 91.89 670 CE1 HIS A 422 48.318 59.473 10.936 1.00 94.70 671 NE2 HIS A 422 49.060 59.300 12.015 1.00 93.25 672 N PRO A 423 48.954 54.871 10.474 1.00 92.64 673 CA PRO A 423 50.209 54.111 10.460 1.00 95.19 674 C PRO A 423 50.838 53.628 11.775 1.00 97.06 675 O PRO A 423 51.064 52.431 11.945 1.00 97.57 676 CB PRO A 423 51.155 55.024 9.667 1.00 95.56 677 CG PRO A 423 50.566 56.391 9.853 1.00 93.94 678 CD PRO A 423 49.105 56.112 9.696 1.00 93.12 679 N HIS A 424 51.105 54.542 12.701 1.00 98.71 680 CA HIS A 424 51.769 54.190 13.957 1.00 100.16 681 C HIS A 424 51.021 53.496 15.095 1.00 99.67 682 O HIS A 424 51.609 52.690 15.816 1.00 99.61 683 CB HIS A 424 52.451 55.435 14.522 1.00 102.42 684 CG HIS A 424 53.475 56.022 13.605 1.00 105.47 685 ND1 HIS A 424 53.372 57.298 13.092 1.00 107.10 686 CD2 HIS A 424 54.639 55.521 13.133 1.00 97.46 687 CE1 HIS A 424 54.430 57.556 12.345 1.00 106.81 688 NE2 HIS A 424 55.215 56.494 12.353 1.00 106.61 689 N LEU A 425 49.742 53.798 15.267 1.00 99.19 690 CA LEU A 425 48.972 53.216 16.363 1.00 99.01 691 C LEU A 425 48.692 51.714 16.284 1.00 98.36 692 O LEU A 425 48.479 51.160 15.204 1.00 98.39 693 CB LEU A 425 47.671 53.994 16.507 1.00 100.66 694 CG LEU A 425 47.969 55.495 16.467 1.00 101.95 695 CD1 LEU A 425 46.683 56.285 16.569 1.00 102.59 696 CD2 LEU A 425 48.923 55.856 17.598 1.00 103.85 697 N PRO A 426 48.685 51.038 17.448 1.00 97.57 698 CA PRO A 426 48.435 49.596 17.540 1.00 96.82 699 C PRO A 426 47.075 49.186 16.992 1.00 95.53 700 O PRO A 426 46.990 48.560 15.937 1.00 95.77 701 CB PRO A 426 48.570 49.318 19.037 1.00 97.13 702 CG PRO A 426 48.106 50.605 19.660 1.00 97.88 703 CG PRO A 426 48.802 51.631 18.793 1.00 97.70 704 N ARG A 427 46.015 49.536 17.713 1.00 94.16 705 CA ARG A 427 44.669 49.198 17.274 1.00 92.52 706 C ARG A 427 44.091 50.315 16.408 1.00 89.85 707 O ARG A 427 44.487 51.477 16.517 1.00 89.26 708 CB ARG A 427 43.749 48.948 18.478 1.00 97.34 709 CG ARG A 427 42.381 48.398 18.077 1.00 99.32 710 CD ARG A 427 41.428 48.193 19.253 1.00 105.99 711 NE ARG A 427 40.197 47.532 18.815 1.00 111.10 712 CZ ARG A 427 39.140 47.298 19.588 1.00 111.66 713 NH1 ARG A 427 39.143 47.673 20.861 1.00 111.70 714 NH2 ARG A 427 38.078 46.679 19.087 1.00 110.09 715 N ALA A 428 43.158 49.949 15.538 1.00 86.56 716 CA ALA A 428 42.513 50.910 14.661 1.00 82.70 717 C ALA A 428 41.389 51.602 15.423 1.00 80.03 718 O ALA A 428 40.711 50.981 16.239 1.00 80.29 719 CB ALA A 428 41.953 50.200 13.437 1.00 83.85 720 N LEU A 429 41.203 52.892 15.164 1.00 76.76 721 CA LEU A 429 40.144 53.651 15.815 1.00 72.72 722 C LEU A 429 38.820 53.289 15.164 1.00 69.67 723 O LEU A 429 38.742 53.128 13.947 1.00 68.64 724 CB LEU A 429 40.392 55.156 15.671 1.00 73.60 725 CG LEU A 429 41.169 55.847 16.793 1.00 73.35 726 CD1 LEU A 429 41.498 57.280 16.404 1.00 72.09 727 CD2 LEU A 429 40.333 55.813 18.065 1.00 76.40 728 N MET A 430 37.779 53.153 15.976 1.00 66.83 729 CA MET A 430 36.468 52.814 15.449 1.00 64.81 730 C MET A 430 35.384 53.678 16.074 1.00 61.41 731 O MET A 430 35.274 53.776 17.299 1.00 60.84 732 CB MET A 430 36.173 51.335 15.691 1.00 68.22 733 CG MET A 430 37.247 50.416 15.133 1.00 74.39 734 SD MET A 430 36.886 48.679 15.387 1.00 83.18 735 CE MET A 430 36.836 48.607 17.194 1.00 84.12 736 N ARG A 431 34.590 54.312 15.218 1.00 57.17 737 CA ARG A 431 33.506 55.172 15.674 1.00 54.04 738 C ARG A 431 32.234 54.752 14.963 1.00 50.58 739 O ARG A 431 32.270 54.367 13.796 1.00 50.46 740 CB ARG A 431 33.825 56.641 15.364 1.00 55.16 741 CG ARG A 431 35.036 57.187 16.109 1.00 59.24 742 CD ARG A 431 34.802 57.172 17.611 1.00 63.93 743 NE ARG A 431 35.983 57.586 18.363 1.00 70.30 744 CZ ARG A 431 36.070 57.557 19.689 1.00 76.24 745 NH1 ARG A 431 35.041 57.131 20.417 1.00 77.83 746 NH2 ARG A 431 37.185 57.952 20.289 1.00 77.12 747 N SER A 432 31.112 54.812 15.669 1.00 46.92 748 CA SER A 432 29.835 54.437 15.084 1.00 45.15 749 C SER A 432 28.784 55.482 15.398 1.00 42.49 750 O SER A 432 28.901 56.218 16.379 1.00 42.76 751 CB SER A 432 29.394 53.068 15.610 1.00 44.31 752 OC SER A 432 29.316 53.084 17.018 1.00 49.96 753 N THR A 433 27.749 55.540 14.570 1.00 40.28 754 CA THR A 433 26.691 56.522 14.763 1.00 39.71 755 C THR A 433 25.356 55.996 14.257 1.00 39.49 756 O THR A 433 25.315 55.186 13.334 1.00 40.22 757 CB THR A 433 27.023 57.839 14.022 1.00 38.07 758 OG1 THR A 433 26.006 58.807 14.295 1.00 39.56 759 CG2 THR A 433 27.088 57.609 12.518 1.00 36.99 760 N THR A 434 24.272 56.461 14.874 1.00 39.18 761 CA THR A 434 22.913 56.068 14.512 1.00 40.70 762 C THR A 434 21.965 57.186 14.934 1.00 40.23 763 O THR A 434 22.364 58.091 15.659 1.00 41.18 764 CB THR A 434 22.484 54.784 15.256 1.00 43.01 765 OG1 THR A 434 22.362 55.052 16.661 1.00 47.85 766 CG2 THR A 434 23.524 53.726 15.105 1.00 48.67 767 N LYS A 435 20.714 57.125 14.496 1.00 40.97 768 CA LYS A 435 19.767 58.150 14.889 1.00 45.73 769 C LYS A 435 19.601 58.021 16.398 1.00 48.93 770 O LYS A 435 19.710 56.930 16.942 1.00 48.49 771 CE LYS A 435 18.434 57.937 14.194 1.00 45.94 772 N THR A 436 19.365 59.133 17.082 1.00 52.01 773 CA THR A 436 19.171 59.080 18.526 1.00 54.88 774 C THR A 436 17.722 58.684 18.774 1.00 55.70 775 O THR A 436 16.823 59.146 18.077 1.00 55.21 776 CB THR A 436 19.438 60.454 19.191 1.00 56.24 777 OG1 THR A 436 20.821 60.802 19.038 1.00 60.56 778 CG2 THR A 436 19.090 60.412 20.677 1.00 57.04 779 N SER A 437 17.501 57.810 19.748 1.00 57.93 780 CA SER A 437 16.149 57.380 20.080 1.00 60.42 781 C SER A 437 15.683 58.239 21.249 1.00 60.49 782 O SER A 437 16.357 59.203 21.623 1.00 60.21 783 CB SER A 437 16.133 55.894 20.470 1.00 61.57 784 OG SER A 437 16.957 55.651 21.600 1.00 65.51 785 N GLY A 438 14.533 57.895 21.821 1.00 60.09 786 CA GLY A 438 14.022 58.666 22.939 1.00 58.42 787 C GLY A 438 12.937 59.630 22.511 1.00 57.80 788 O GLY A 438 12.648 59.747 21.322 1.00 56.51 789 N PRO A 439 12.309 60.333 23.467 1.00 57.81 790 CA PRO A 439 11.242 61.295 23.185 1.00 56.19 791 C PRO A 439 11.692 62.422 22.263 1.00 53.91 792 O PRO A 439 12.886 62.709 22.147 1.00 53.91 793 CE PRO A 439 10.865 61.806 24.576 1.00 57.79 794 CG PRO A 439 11.147 60.633 25.448 1.00 58.60 795 CD PRO A 439 12.485 60.173 24.921 1.00 60.65 796 N ARG A 440 10.722 63.055 21.612 1.00 51.09 797 CA ARG A 440 10.990 64.163 20.702 1.00 48.90 798 C ARG A 440 10.220 65.365 21.231 1.00 45.83 799 O ARG A 440 9.188 65.202 21.881 1.00 45.88 800 CE ARG A 440 10.501 63.836 19.289 1.00 49.95 801 CG ARG A 440 10.919 62.473 18.771 1.00 59.03 802 CD ARG A 440 12.406 62.373 18.448 1.00 65.31 803 NE ARG A 440 12.814 60.973 18.342 1.00 72.31 804 CZ ARG A 440 13.986 60.553 17.878 1.00 74.99 804 CZ ARG A 440 13.986 60.553 17.878 1.00 74.99 805 NH1 ARG A 440 14.894 61.419 17.460 1.00 77.22 806 NH2 ARG A 440 14.252 59.255 17.837 1.00 78.59 807 N ALA A 441 10.727 66.564 20.957 1.00 42.09 808 CA ALA A 441 10.079 67.800 21.387 1.00 39.26 809 C ALA A 441 10.476 68.894 20.413 1.00 38.22 810 O ALA A 441 11.649 69.034 20.076 1.00 38.95 811 CE ALA A 441 10.511 68.170 22.798 1.00 36.56 812 N ALA A 442 9.496 69.666 19.966 1.00 37.22 813 CA ALA A 442 9.739 70.729 19.011 1.00 37.60 814 C ALA A 442 10.550 71.879 19.590 1.00 38.65 815 O ALA A 442 10.553 72.103 20.798 1.00 40.22 816 CB ALA A 442 8.415 71.248 18.481 1.00 37.17 817 N PRO A 443 11.260 72.619 18.722 1.00 38.04 818 CA PRO A 443 12.089 73.765 19.104 1.00 36.79 819 C PRO A 443 11.224 75.019 19.243 1.00 38.14 820 O PRO A 443 10.236 75.174 18.521 1.00 37.39 821 CB PRO A 443 13.050 73.923 17.921 1.00 36.30 822 CG PRO A 443 12.946 72.632 17.159 1.00 36.35 823 CD PRO A 443 11.512 72.249 17.320 1.00 37.85 824 N GLU A 444 11.594 75.894 20.173 1.00 36.28 825 CA GLU A 444 10.901 77.163 20.371 1.00 35.57 826 C GLU A 444 11.941 78.171 19.888 1.00 33.87 827 O GLU A 444 13.110 78.105 20.291 1.00 33.43 828 CB GLU A 444 10.580 77.383 21.851 1.00 38.68 829 N VAL A 445 11.520 79.097 19.033 1.00 30.18 830 CA VAL A 445 12.432 80.070 18.450 1.00 28.24 831 C VAL A 445 12.136 81.523 18.811 1.00 28.44 832 O VAL A 445 11.000 81.975 18.721 1.00 26.78 833 CB VAL A 445 12.417 79.937 16.905 1.00 28.10 834 CG1 VAL A 445 13.370 80.933 16.274 1.00 25.56 835 CG2 VAL A 445 12.771 78.521 16.511 1.00 26.30 836 N TYR A 446 13.175 82.251 19.203 1.00 27.87 837 CA TYR A 446 13.019 83.651 19.551 1.00 27.91 838 C TYR A 446 14.193 84.460 19.024 1.00 27.06 839 O TYR A 446 15.326 84.307 19.480 1.00 27.96 840 CB TYR A 446 12.898 83.836 21.074 1.00 26.45 841 CG TYR A 446 12.749 85.289 21.447 1.00 26.59 842 CD1 TYR A 446 11.714 86.057 20.905 1.00 28.48 843 CD2 TYR A 446 13.659 85.914 22.305 1.00 29.02 844 CE1 TYR A 446 11.589 87.417 21.204 1.00 33.24 845 CE2 TYR A 446 13.543 87.274 22.616 1.00 31.33 846 CZ TYR A 446 12.506 88.015 22.059 1.00 36.01 847 OH TYR A 446 12.387 89.352 22.338 1.00 36.54 848 N ALA A 447 13.914 85.326 18.060 1.00 28.07 849 CA ALA A 447 14.949 86.150 17.439 1.00 27.67 850 C ALA A 447 14.815 87.579 17.932 1.00 29.19 851 O ALA A 447 13.702 88.036 18.173 1.00 31.10 852 CB ALA A 447 14.802 86.098 15.931 1.00 23.97 853 N PHE A 448 15.929 88.293 18.079 1.00 29.56 854 CA PHE A 448 15.849 89.657 18.578 1.00 32.50 855 C PHE A 448 17.075 90.483 18.246 1.00 33.67 856 O PHE A 448 18.112 89.950 17.872 1.00 35.26 857 CB PHE A 448 15.659 89.630 20.097 1.00 35.29 858 CG PHE A 448 16.849 89.077 20.838 1.00 37.04 859 CD1 PHE A 448 17.912 89.909 21.195 1.00 36.66 860 CD2 PHE A 448 16.934 87.714 21.127 1.00 34.95 861 CE1 PHE A 448 19.049 89.382 21.824 1.00 40.91 862 CE2 PHE A 448 18.066 87.178 21.753 1.00 35.99 863 CZ PHE A 448 19.123 88.014 22.103 1.00 35.15 864 N ALA A 449 16.952 91.796 18.396 1.00 35.81 865 CA ALA A 449 18.066 92.693 18.131 1.00 37.63 866 C ALA A 449 18.617 93.253 19.438 1.00 40.96 867 O ALA A 449 17.885 93.441 20.403 1.00 40.14 868 CB ALA A 449 17.623 93.831 17.230 1.00 33.60 869 N THR A 450 19.918 93.509 19.448 1.00 45.40 870 CA THR A 450 20.606 94.071 20.595 1.00 50.82 871 C THR A 450 20.515 95.597 20.498 1.00 53.78 872 O THR A 450 20.673 96.169 19.417 1.00 54.14 873 CB THR A 450 22.090 93.665 20.587 1.00 51.45 874 OG1 THR A 450 22.192 92.242 20.450 1.00 54.12 875 CG2 THR A 450 22.769 94.093 21.877 1.00 55.58 876 N PRO A 451 20.260 96.275 21.626 1.00 56.74 877 CA PRO A 451 20.157 97.737 21.623 1.00 59.05 878 C PRO A 451 21.427 98.391 21.080 1.00 61.00 879 O PRO A 451 22.535 98.080 21.521 1.00 59.71 880 CB PRO A 451 19.933 98.073 23.098 1.00 60.52 881 CC PRO A 451 19.262 96.851 23.640 1.00 61.14 882 CD PRO A 451 20.049 95.739 22.981 1.00 59.39 883 N GLU A 452 21.272 99.285 20.112 1.00 64.30 884 CA GLU A 452 22.428 99.975 19.558 1.00 69.17 885 C GLU A 452 22.252 101.463 19.842 1.00 72.61 886 O GLU A 452 21.667 102.206 19.057 1.00 73.59 887 CB GLU A 452 22.560 99.712 18.054 1.00 65.66 888 CG GLU A 452 24.015 99.566 17.577 1.00 61.46 889 CD GLU A 452 24.717 98.317 18.133 1.00 60.52 890 OE1 GLU A 452 24.053 97.264 18.251 1.00 63.47 891 OE2 GLU A 452 25.934 98.373 18.433 1.00 53.34 892 N TRP A 453 22.763 101.869 20.997 1.00 76.75 893 CA TRP A 453 22.693 103.242 21.481 1.00 81.00 894 C TRP A 453 23.886 104.027 20.913 1.00 82.30 895 O TRP A 453 25.038 103.710 21.215 1.00 82.08 896 CB TRP A 453 22.737 103.191 23.010 1.00 85.65 897 CG TRP A 453 22.182 104.367 23.734 1.00 89.76 898 CD1 TRP A 453 20.939 104.921 23.588 1.00 92.34 899 CD2 TRP A 453 22.819 105.083 24.795 1.00 94.15 900 NE1 TRP A 453 20.764 105.934 24.502 1.00 94.99 901 CE2 TRP A 453 21.904 106.055 25.255 1.00 95.56 902 CE3 TRP A 453 24.079 104.995 25.407 1.00 95.36 903 CZ2 TRP A 453 22.208 106.935 26.300 1.00 97.14 904 CZ3 TRP A 453 24.380 105.869 26.445 1.00 95.61 905 CH2 TRP A 453 23.447 106.826 26.880 1.00 97.12 906 N PRO A 454 23.619 105.058 20.080 1.00 84.10 907 CA PRO A 454 24.606 105.931 19.422 1.00 87.24 908 C PRO A 454 25.892 106.316 20.162 1.00 90.52 909 O PRO A 454 26.088 105.978 21.333 1.00 89.75 910 CB PRO A 454 23.775 107.150 18.988 1.00 84.91 911 CG PRO A 454 22.475 107.017 19.740 1.00 83.62 912 CD PRO A 454 22.259 105.537 19.793 1.00 84.60 913 N GLY A 455 26.751 107.055 19.464 1.00 91.72 914 CA GLY A 455 28.048 107.413 20.012 1.00 94.13 915 C GLY A 455 28.730 106.132 19.601 1.00 96.28 916 O GLY A 455 28.613 105.125 20.301 1.00 97.74 917 N SER A 456 29.442 106.142 18.478 1.00 99.11 918 CA SER A 456 29.974 104.869 18.023 1.00 96.15 919 C SER A 456 31.407 104.465 17.676 1.00 91.50 920 O SER A 456 32.292 105.284 17.333 1.00 88.52 921 CB SER A 456 29.092 104.378 16.879 1.00 95.05 922 OG SER A 456 28.910 105.375 15.884 1.00 110.76 923 N ARG A 457 31.541 103.136 17.752 1.00 87.73 924 CA ARG A 457 32.664 102.251 17.520 1.00 87.81 925 C ARG A 457 31.678 101.103 17.647 1.00 86.30 926 O ARG A 457 31.026 100.998 18.697 1.00 90.57 927 CB ARG A 457 33.634 102.261 18.675 1.00 94.67 928 N ASP A 458 31.512 100.259 16.627 1.00 87.32 929 CA ASP A 458 30.441 99.286 16.780 1.00 80.43 930 C ASP A 458 30.422 97.963 16.080 1.00 72.83 931 O ASP A 458 31.410 97.437 15.599 1.00 73.96 932 CB ASP A 458 29.150 99.985 16.385 1.00 83.19 933 CG ASP A 458 29.102 100.300 14.890 1.00 85.09 934 OD1 ASP A 458 30.065 100.906 14.378 1.00 91.25 935 OD2 ASP A 458 28.108 99.939 14.217 1.00 90.84 936 N LYS A 459 29.196 97.451 16.076 1.00 66.05 937 CA LYS A 459 28.782 96.211 15.437 1.00 61.75 938 C LYS A 459 27.368 95.983 15.886 1.00 56.14 939 O LYS A 459 27.144 95.648 17.046 1.00 56.54 940 CB LYS A 459 29.641 95.031 15.889 1.00 68.18 941 CG LYS A 459 30.801 94.804 14.969 1.00 71.85 942 CD LYS A 459 30.406 94.863 13.499 1.00 73.79 943 CE LYS A 459 31.655 94.839 12.626 1.00 76.14 944 NZ LYS A 459 31.341 94.675 11.169 1.00 79.35 945 N ARG A 460 26.406 96.194 15.001 1.00 52.32 946 CA ARG A 460 25.035 95.951 15.377 1.00 47.59 947 C ARG A 460 24.860 94.436 15.290 1.00 43.34 948 O ARG A 460 25.477 93.761 14.462 1.00 40.40 949 CB ARG A 460 24.104 96.726 14.456 1.00 49.27 950 CG ARG A 460 24.275 98.216 14.671 1.00 56.23 951 CD ARG A 460 23.659 99.006 13.532 1.00 63.20 952 NE ARG A 460 23.997 100.426 13.596 1.00 68.02 953 CZ ARG A 460 25.145 100.955 13.180 1.00 70.46 954 NH1 ARG A 460 26.094 100.185 12.656 1.00 72.23 955 NH2 ARG A 460 25.336 102.264 13.285 1.00 73.53 956 N THR A 461 24.062 93.910 16.198 1.00 39.19 957 CA THR A 461 23.879 92.474 16.278 1.00 36.81 958 C THR A 461 22.447 92.004 16.401 1.00 34.03 959 O THR A 461 21.631 92.607 17.110 1.00 33.96 960 CB THR A 461 24.603 91.890 17.512 1.00 39.13 961 OG1 THR A 461 25.957 92.357 17.557 1.00 46.04 962 CG2 THR A 461 24.630 90.380 17.421 1.00 45.48 963 N LEU A 462 22.157 90.904 15.714 1.00 29.84 964 CA LEU A 462 20.853 90.267 15.788 1.00 28.03 965 C LEU A 462 21.205 88.926 16.410 1.00 27.33 966 O LEU A 462 22.307 88.414 16.207 1.00 24.47 967 CB LEU A 462 20.223 90.074 14.403 1.00 25.97 968 CG LEU A 462 19.888 91.362 13.635 1.00 33.39 969 CO1 LEU A 462 19.172 91.007 12.319 1.00 32.36 970 CD2 LEU A 462 19.014 92.263 14.483 1.00 30.72 971 N ALA A 463 20.286 88.359 17.178 1.00 25.83 972 CA ALA A 463 20.577 87.111 17.836 1.00 25.65 973 C ALA A 463 19.330 86.279 17.957 1.00 26.32 974 O ALA A 463 18.214 86.790 17.846 1.00 27.53 975 CB ALA A 463 21.179 87.381 19.212 1.00 28.15 976 N CYS A 464 19.518 84.992 18.195 1.00 21.23 977 CA CYS A 464 18.388 84.093 18.276 1.00 24.77 978 C CYS A 464 18.599 83.016 19.314 1.00 22.14 979 O CYS A 464 19.683 82.431 19.402 1.00 24.66 980 CB CYS A 464 18.193 83.429 16.914 1.00 22.04 981 SG CYS A 464 16.790 82.298 16.720 1.00 34.06 982 N LEU A 465 17.548 82.741 20.075 1.00 22.44 983 CA LEU A 465 17.598 81.697 21.089 1.00 23.11 984 C LEU A 465 16.644 80.615 20.641 1.00 22.43 985 O LEU A 465 15.483 80.898 20.352 1.00 23.73 986 CB LEU A 465 17.155 82.230 22.461 1.00 22.99 987 CG LEU A 465 16.810 81.177 23.538 1.00 19.04 988 CD1 LEU A 465 18.035 80.331 23.866 1.00 21.72 989 CD2 LEU A 465 16.347 81.884 24.818 1.00 28.23 990 N ILE A 466 17.125 79.380 20.581 1.00 22.56 991 CA ILE A 466 16.277 78.268 20.169 1.00 22.11 992 C ILE A 466 16.302 77.256 21.297 1.00 24.25 993 O ILE A 466 17.375 76.815 21.706 1.00 24.93 994 CB ILE A 466 16.781 77.654 18.861 1.00 22.15 995 CG1 ILE A 466 16.849 78.750 17.786 1.00 23.07 996 CG2 ILE A 466 15.822 76.525 18.416 1.00 25.24 997 CD1 ILE A 466 17.509 78.318 16.496 1.00 33.12 998 N GLN A 467 15.132 76.863 21.793 1.00 24.63 999 CA GLN A 467 15.120 75.970 22.951 1.00 28.64 1000 C GLN A 467 13.982 74.963 23.072 1.00 31.08 1001 O GLN A 467 13.071 74.915 22.235 1.00 31.00 1002 CB GLN A 467 15.172 76.830 24.228 1.00 25.58 1003 CG GLN A 467 13.943 77.727 24.404 1.00 25.53 1004 CD GLN A 467 14.044 78.693 25.599 1.00 30.72 1005 OE1 GLN A 467 14.790 78.456 26.549 1.00 29.76 1006 NE2 GLN A 467 13.273 79.779 25.550 1.00 32.18 1007 N ASN A 468 14.083 74.147 24.123 1.00 33.71 1008 CA ASN A 468 13.114 73.106 24.459 1.00 36.96 1009 C ASN A 468 12.993 71.999 23.423 1.00 38.20 1010 O ASN A 468 11.931 71.392 23.288 1.00 38.39 1011 CB ASN A 468 11.731 73.719 24.676 1.00 41.06 1012 CG ASN A 468 11.748 74.837 25.686 1.00 46.41 1013 OD1 ASN A 468 12.372 74.721 26.741 1.00 50.82 1014 ND2 ASN A 468 11.052 75.928 25.376 1.00 53.31 1015 N PHE A 469 14.065 71.732 22.685 1.00 35.74 1016 CA PHE A 469 14.003 70.690 21.677 1.00 33.87 1017 C PHE A 469 14.804 69.453 22.056 1.00 33.63 1018 O PHE A 469 15.727 69.513 22.860 1.00 34.78 1019 CB PHE A 469 14.495 71.228 20.322 1.00 29.12 1020 CG PHE A 469 15.926 71.691 20.334 1.00 26.27 1021 CO1 PHE A 469 16.959 70.792 20.133 1.00 22.45 1022 CD2 PHE A 469 16.238 73.034 20.539 1.00 22.06 1023 CE1 PHE A 469 18.285 71.214 20.126 1.00 23.84 1024 CE2 PHE A 469 17.564 73.465 20.536 1.00 28.02 1025 CZ PHE A 469 18.593 72.549 20.327 1.00 23.33 1026 N MET A 470 14.431 68.327 21.466 1.00 35.64 1027 CA MET A 470 15.120 67.065 21.687 1.00 37.62 1028 C MET A 470 14.684 66.104 20.596 1.00 36.36 1029 O MET A 470 13.529 66.122 20.177 1.00 36.33 1030 CB MET A 470 14.804 66.495 23.076 1.00 42.61 1031 CG MET A 470 13.354 66.179 23.350 1.00 50.60 1032 SD MET A 470 13.141 65.744 25.113 1.00 66.08 1033 CE MET A 470 13.780 64.056 25.134 1.00 66.35 1034 N PRO A 471 15.613 65.283 20.079 1.00 34.63 1035 CA PRO A 471 17.039 65.169 20.418 1.00 32.61 1036 C PRO A 471 17.818 66.453 20.143 1.00 31.92 1037 O PRO A 471 17.244 67.436 19.685 1.00 29.59 1038 CB PRO A 471 17.520 64.015 19.538 1.00 33.95 1039 CG PRO A 471 16.277 63.227 19.295 1.00 37.90 1040 CD PRO A 471 15.246 64.291 19.058 1.00 34.78 1041 N GLU A 472 19.128 66.413 20.386 1.00 32.28 1042 CA GLU A 472 20.001 67.580 20.234 1.00 36.49 1043 C GLU A 472 20.380 68.043 18.830 1.00 35.52 1044 O GLU A 472 20.870 69.162 18.683 1.00 34.87 1045 CB GLU A 472 21.302 67.377 21.015 1.00 41.97 1046 CG GLU A 472 22.213 66.306 20.423 1.00 54.78 1047 CD GLU A 472 23.527 66.144 21.184 1.00 62.41 1048 OE1 GLU A 472 23.603 66.579 22.356 1.00 67.26 1O49 OE2 GLU A 472 24.481 65.566 20.613 1.00 64.96 1050 N ASP A 473 20.161 67.221 17.805 1.00 34.38 1051 CA ASP A 473 20.543 67.629 16.452 1.00 31.83 1052 C ASP A 473 19.602 68.686 15.886 1.00 31.24 1053 O ASP A 473 18.380 68.528 15.901 1.00 31.80 1054 CB ASP A 473 20.621 66.420 15.516 1.00 34.73 1055 CG ASP A 473 21.746 65.453 15.904 1.00 40.83 1056 OD1 ASP A 473 22.841 65.924 16.296 1.00 44.18 1057 OD2 ASP A 473 21.539 64.222 15.810 1.00 40.17 1058 N ILE A 474 20.184 69.774 15.398 1.00 26.96 1059 CA ILE A 474 19.393 70.856 14.854 1.00 25.39 1060 C ILE A 474 20.225 71.715 13.892 1.00 24.74 1061 O ILE A 474 21.436 71.824 14.031 1.00 25.20 1062 CB ILE A 474 18.842 71.738 16.008 1.00 23.81 1063 CG1 ILE A 474 17.748 72.675 15.502 1.00 22.23 1064 CG2 ILE A 474 19.974 72.538 16.647 1.00 27.10 1065 CO1 ILE A 474 17.064 73.456 16.650 1.00 25.30 1066 N SER A 475 19.570 72.288 12.891 1.00 23.27 1067 CA SER A 475 20.252 73.170 11.952 1.00 22.17 1068 C SER A 475 19.609 74.534 12.148 1.00 21.71 1069 O SER A 475 18.393 74.649 12.224 1.00 20.84 1070 CB SER A 475 20.049 72.721 10.507 1.00 20.43 1071 OG SER A 475 20.589 71.436 10.294 1.00 30.00 1072 N VAL A 476 20.442 75.558 12.213 1.00 21.76 1073 CA VAL A 476 19.980 76.906 12.425 1.00 21.72 1074 C VAL A 476 20.435 77.725 11.249 1.00 23.56 1075 O VAL A 476 21.555 77.564 10.780 1.00 25.95 1076 CB VAL A 476 20.606 77.513 13.715 1.00 21.56 1077 CO1 VAL A 476 20.157 78.975 13.878 1.00 18.70 1078 CG2 VAL A 476 20.197 76.685 14.934 1.00 20.99 1079 N GLN A 477 19.574 78.606 10.764 1.00 25.16 1080 CA GLN A 477 19.965 79.428 9.640 1.00 26.65 1081 C GLN A 477 19.263 80.767 9.662 1.00 26.62 1082 O GLN A 477 18.160 80.891 10.175 1.00 26.40 1083 CB GLN A 477 19.701 78.683 8.325 1.00 31.51 1084 CG GLN A 477 18.289 78.252 8.089 1.00 44.27 1085 CD GLN A 477 18.188 77.095 7.084 1.00 47.76 1086 DE1 GLN A 477 17.104 76.786 6.598 1.00 50.57 1087 NE2 GLN A 477 19.317 76.449 6.787 1.00 47.32 1088 N TRP A 478 19.941 81.780 9.146 1.00 27.41 1089 CA TRP A 478 19.375 83.112 9.074 1.00 28.36 1090 C TRP A 478 18.944 83.408 7.635 1.00 30.10 1091 O TRP A 478 19.567 82.940 6.672 1.00 25.31 1092 CB TRP A 478 20.404 84.139 9.533 1.00 28.76 1093 CG TRP A 478 20.649 84.098 11.013 1.00 34.11 1094 CD1 TRP A 478 21.522 83.287 11.685 1.00 31.25 1095 CD2 TRP A 478 19.980 84.878 12.006 1.00 31.01 1096 NE1 TRP A 478 21.436 83.515 13.031 1.00 27.71 1097 CE2 TRP A 478 20.496 84.487 13.259 1.00 31.95 1098 CE3 TRP A 478 18.993 85.871 11.960 1.00 34.16 1099 CZ2 TRP A 478 20.055 85.058 14.463 1.00 25.26 1100 CZ3 TRP A 478 18.556 86.439 13.153 1.00 31.64 1101 CH2 TRP A 478 19.089 86.029 14.387 1.00 28.89 1102 N LEU A 479 17.877 84.182 7.498 1.00 32.48 1103 CA LEU A 479 17.355 84.551 6.187 1.00 37.36 1104 C LEU A 479 16.943 86.016 6.140 1.00 40.42 1105 O LEU A 479 16.448 86.560 7.123 1.00 40.14 1106 CE LEU A 479 16.122 83.722 5.848 1.00 39.83 1107 CG LEU A 479 16.044 82.254 6.258 1.00 44.57 1108 CD1 LEU A 479 14.713 81.710 5.810 1.00 52.98 1109 CD2 LEU A 479 17.161 81.470 5.634 1.00 50.71 1110 N HIS A 480 17.152 86.653 4.998 1.00 43.05 1111 CA HIS A 480 16.723 88.028 4.824 1.00 49.20 1112 C HIS A 480 15.464 87.854 3.984 1.00 52.73 1113 O HIS A 480 15.509 87.895 2.753 1.00 52.90 1114 CB HIS A 480 17.756 88.846 4.057 1.00 52.25 1115 CD HIS A 480 17.330 90.259 3.814 1.00 57.22 1116 ND1 HIS A 480 17.525 91.263 4.736 1.00 61.37 1117 CD2 HIS A 480 16.658 90.822 2.781 1.00 59.16 1118 CE1 HIS A 480 16.993 92.384 4.285 1.00 59.88 1119 NE2 HIS A 480 16.460 92.144 3.100 1.00 66.11 1120 N ASN A 481 14.347 87.629 4.670 1.00 56.65 1121 CA ASN A 481 13.057 87.394 4.030 1.00 59.93 1122 C ASN A 481 13.009 85.940 3.581 1.00 59.65 1123 O ASN A 481 13.031 85.029 4.405 1.00 61.04 1124 CB ASN A 481 12.849 88.312 2.818 1.00 64.65 1125 CG ASN A 481 12.578 89.748 3.210 1.00 72.38 1126 OD1 ASN A 481 11.636 90.037 3.953 1.00 74.96 1127 ND2 ASN A 481 13.401 90.662 2.707 1.00 75.60 1128 N GLU A 482 12.975 85.728 2.273 1.00 58.97 1129 CA GLU A 482 12.903 84.387 1.704 1.00 58.55 1130 C GLU A 482 14.254 83.785 1.318 1.00 55.30 1131 O GLU A 482 14.347 82.587 1.056 1.00 57.27 1132 CE GLU A 482 11.993 84.424 0.473 1.00 65.42 1133 CD GLU A 482 11.787 85.840 0.072 1.00 73.94 1134 CD GLU A 482 11.127 85.865 1.432 1.00 80.29 1135 OE1 GLU A 482 11.770 85.432 2.413 1.00 86.31 1136 OE2 GLU A 482 9.967 86.316 1.520 1.00 82.73 1137 N VAL A 483 15.299 84.603 1.286 1.00 50.25 1138 CA VAL A 483 16.612 84.113 0.889 1.00 45.78 1139 C VAL A 483 17.575 83.867 2.048 1.00 43.04 1140 O VAL A 483 17.766 84.720 2.902 1.00 41.34 1141 CE VAL A 483 17.261 85.073 0.133 1.00 43.76 1142 CG1 VAL A 483 17.317 86.471 0.432 1.00 46.25 1143 CG2 VAL A 483 18.654 84.589 0.494 1.00 41.37 1144 N GLN A 484 18.188 82.688 2.050 1.00 42.30 1145 CA GLN A 484 19.126 82.300 3.095 1.00 43.21 1146 C GLN A 484 20.509 82.942 2.959 1.00 42.48 1147 O GLN A 484 21.055 83.062 1.856 1.00 41.64 1148 CE GLN A 484 19.269 80.774 3.129 1.00 45.96 1149 CG GLN A 484 20.331 80.276 4.101 1.00 54.43 1150 CD GLN A 484 20.427 78.760 4.159 1.00 59.02 1151 OE1 GLN A 484 21.400 78.209 4.677 1.00 59.71 1152 NE2 GLN A 484 19.410 78.078 3.636 1.00 61.46 1153 N LEU A 485 21.061 83.361 4.094 1.00 38.99 1154 CA LEU A 485 22.382 83.982 4.147 1.00 39.17 1155 C LEU A 485 23.458 82.900 4.247 1.00 40.35 1156 O LEU A 485 23.183 81.778 4.670 1.00 37.39 1157 CE LEU A 485 22.493 84.895 5.375 1.00 37.16 1158 CD LEU A 485 21.460 86.021 5.498 1.00 39.66 1159 CD1 LEU A 485 21.670 86.764 6.807 1.00 39.30 1160 CD2 LEU A 485 21.580 86.956 4.305 1.00 40.56 1161 N PRO A 486 24.700 83.227 3.858 1.00 42.55 1162 CA PRO A 486 25.772 82.234 3.942 1.00 46.30 1163 C PRO A 486 25.940 81.850 5.412 1.00 49.32 1164 O PRO A 486 25.748 82.684 6.294 1.00 48.81 1165 CB PRO A 486 26.991 82.994 3.425 1.00 45.64 1166 CG PRO A 486 26.413 84.068 2.572 1.00 45.29 1167 CD PRO A 486 25.206 84.505 3.331 1.00 40.65 1168 N ASP A 487 26.310 80.603 5.671 1.00 53.39 1169 CA ASP A 487 26.507 80.135 7.038 1.00 57.75 1170 C ASP A 487 27.603 80.940 7.750 1.00 57.25 1171 O ASP A 487 27.424 81.395 8.887 1.00 57.75 1172 CB ASP A 487 26.892 78.656 7.023 1.00 67.82 1173 CG ASP A 487 26.821 78.023 8.397 1.00 76.17 1174 OD1 ASP A 487 27.291 78.655 9.366 1.00 84.77 1175 OD2 ASP A 487 26.303 76.889 8.508 1.00 86.94 1176 N ALA A 488 28.727 81.122 7.065 1.00 54.64 1177 CA ALA A 488 29.871 81.848 7.607 1.00 53.45 1178 C ALA A 488 29.531 83.179 8.263 1.00 52.74 1179 O ALA A 488 30.359 83.757 8.966 1.00 53.06 1180 CB ALA A 488 30.892 82.070 6.515 1.00 53.75 1181 N ARG A 489 28.313 83.662 8.044 1.00 50.96 1182 CA ARG A 489 27.896 84.940 8.609 1.00 47.84 1183 C ARG A 489 27.436 84.895 10.064 1.00 45.10 1184 O ARG A 489 27.442 85.919 10.737 1.00 43.37 1185 CB ARG A 489 26.792 85.554 7.746 1.00 48.99 1186 CG ARG A 489 27.306 86.368 6.576 1.00 50.01 1187 CD ARG A 489 27.173 87.839 6.873 1.00 50.36 1188 NE ARG A 489 26.019 88.413 6.195 1.00 56.65 1189 CZ ARG A 489 25.434 89.552 6.543 1.00 58.23 1190 NH1 ARG A 489 25.886 90.248 7.578 1.00 61.07 1191 NH2 ARG A 489 24.407 90.006 5.840 1.00 59.63 1192 N HIS A 490 27.027 83.728 10.549 1.00 42.41 1193 CA HIS A 490 26.576 83.635 11.934 1.00 41.63 1194 C HIS A 490 27.390 82.648 12.766 1.00 39.71 1195 O HIS A 490 28.129 81.832 12.235 1.00 41.30 1196 CB HIS A 490 25.092 83.252 12.000 1.00 42.40 1197 CC HIS A 490 24.793 81.880 11.486 1.00 43.27 1198 ND1 HIS A 490 24.423 81.634 10.181 1.00 42.27 1199 CD2 HIS A 490 24.821 80.674 12.101 1.00 44.41 1200 CE1 HIS A 490 24.236 80.338 10.014 1.00 39.88 1201 NE2 HIS A 490 24.470 79.732 11.166 1.00 45.37 1202 N SER A 491 27.245 82.742 14.080 1.00 37.20 1203 CA SER A 491 27.946 81.866 15.005 1.00 36.36 1204 C SER A 491 26.915 81.199 15.927 1.00 33.06 1205 O SER A 491 26.172 81.879 16.639 1.00 33.77 1206 CB SER A 491 28.949 82.690 15.812 1.00 35.42 1207 OC SER A 491 29.547 81.906 16.818 1.00 43.65 1208 N THR A 492 26.878 79.872 15.912 1.00 29.90 1209 CA THR A 492 25.927 79.105 16.717 1.00 29.91 1210 C THR A 492 26.623 78.278 17.813 1.00 29.20 1211 O THR A 492 27.609 77.604 17.548 1.00 30.85 1212 CE THR A 492 25.094 78.153 15.802 1.00 29.85 1213 OC1 THR A 492 24.403 78.930 14.819 1.00 35.86 1214 CC2 THR A 492 24.059 77.366 16.602 1.00 28.05 1215 N THR A 493 26.095 78.319 19.035 1.00 29.49 1216 CA THR A 493 26.687 77.568 20.143 1.00 30.19 1217 C THR A 493 26.305 76.099 20.044 1.00 32.39 1218 O THR A 493 25.390 75.737 19.314 1.00 30.70 1219 CB THR A 493 26.222 78.098 21.532 1.00 27.82 1220 OC1 THR A 493 24.794 78.008 21.640 1.00 30.48 1221 CC2 THR A 493 26.647 79.533 21.728 1.00 22.03 1222 N GLN A 494 27.014 75.253 20.778 1.00 35.09 1223 CA GLN A 494 26.721 73.821 20.770 1.00 38.19 1224 C GLN A 494 25.509 73.568 21.651 1.00 36.48 1225 O GLN A 494 25.330 74.240 22.668 1.00 35.75 1226 CB GLN A 494 27.904 73.019 21.325 1.00 43.09 1227 CG GLN A 494 29.167 73.098 20.490 1.00 58.35 1228 CD GLN A 494 28.934 72.671 19.058 1.00 65.11 1229 OE1 GLN A 494 28.391 71.597 18.797 1.00 71.67 1230 NE2 GLN A 494 29.345 73.512 18.118 1.00 71.87 1231 N PRO A 495 24.661 72.598 21.272 1.00 36.89 1232 CA PRO A 495 23.470 72.278 22.063 1.00 38.37 1233 C PRO A 495 23.863 71.991 23.513 1.00 40.80 1234 O PRO A 495 24.837 71.286 23.773 1.00 40.76 1235 CB PRO A 495 22.920 71.043 21.371 1.00 37.83 1236 CD PRO A 495 23.300 71.285 19.926 1.00 40.41 1237 CD PRO A 495 24.716 71.791 20.039 1.00 35.81 1238 N ARG A 496 23.120 72.560 24.450 1.00 42.05 1239 CA ARG A 496 23.392 72.345 25.860 1.00 47.69 1240 C ARG A 496 22.146 71.828 26.558 1.00 51.66 1241 O ARG A 496 21.042 72.317 26.316 1.00 51.95 1242 CB ARG A 496 23.849 73.646 26.516 1.00 45.81 1243 CG ARG A 496 25.283 74.001 26.208 1.00 51.53 1244 CD ARG A 496 25.653 75.383 26.709 1.00 53.72 1245 NE ARG A 496 27.046 75.425 27.137 1.00 57.50 1246 CZ ARG A 496 27.478 74.992 28.317 1.00 58.59 1247 NH1 ARG A 496 26.626 74.489 29.199 1.00 57.22 1248 NE2 ARG A 496 28.768 75.058 28.612 1.00 65.31 1249 N LYS A 497 22.319 70.827 27.413 1.00 56.98 1250 CA LYS A 497 21.192 70.265 28.147 1.00 61.91 1251 C LYS A 497 20.733 71.299 29.145 1.00 63.97 1252 O LYS A 497 21.405 72.300 29.371 1.00 64.61 1253 CD LYS A 497 21.597 69.013 28.928 1.00 66.35 1254 CG LYS A 497 21.819 67.752 28.113 1.00 74.14 1255 CD LYS A 497 22.241 66.607 29.034 1.00 80.69 1256 CE LYS A 497 22.408 65.296 28.286 1.00 84.48 1257 NZ LYS A 497 22.861 64.215 29.211 1.00 88.26 1258 N THR A 498 19.583 71.045 29.748 1.00 67.67 1259 CA THR A 498 19.028 71.931 30.758 1.00 71.26 1260 C THR A 498 18.316 71.050 31.760 1.00 73.04 1261 O THR A 498 18.610 69.857 31.864 1.00 72.83 1262 CB THR A 498 18.015 72.921 30.155 1.00 71.80 1263 OG1 THR A 498 17.045 72.208 29.379 1.00 71.58 1264 CG2 THR A 498 18.722 73.930 29.281 1.00 73.61 1265 N LYS A 499 17.380 71.638 32.495 1.00 75.57 1266 CA LYS A 499 16.607 70.895 33.480 1.00 77.62 1267 C LYS A 499 15.458 70.173 32.779 1.00 77.92 1268 O LYS A 499 14.504 70.809 32.332 1.00 79.19 1269 CD LYS A 499 16.042 71.848 34.533 1.00 80.22 1270 CG LYS A 499 17.069 72.428 35.496 1.00 81.04 1271 CD LYS A 499 17.507 71.397 36.529 1.00 83.26 1272 CE LYS A 499 18.368 72.031 37.613 1.00 84.81 1273 NZ LYS A 499 18.736 71.055 38.675 1.00 86.04 1274 N GLY A 500 15.566 68.852 32.667 1.00 76.91 1275 CA GLY A 500 14.523 68.056 32.039 1.00 75.83 1276 C GLY A 500 14.040 68.459 30.655 1.00 75.14 1277 O GLY A 500 14.024 67.629 29.745 1.00 75.52 1278 N SER A 501 13.642 69.718 30.495 1.00 73.08 1279 CA SER A 501 13.132 70.230 29.225 1.00 71.65 1280 C SER A 501 13.764 69.592 27.994 1.00 68.64 1281 O SER A 501 13.085 68.910 27.223 1.00 71.13 1282 CB SER A 501 13.321 71.746 29.147 1.00 74.43 1283 OG SER A 501 14.667 72.076 28.859 1.00 80.92 1284 N GLY A 502 15.060 69.814 27.810 1.00 63.14 1285 CA GLY A 502 15.741 69.256 26.657 1.00 54.62 1286 C GLY A 502 16.982 70.048 26.297 1.00 48.04 1287 O GLY A 502 17.917 70.131 27.094 1.00 48.08 1288 N PHE A 503 17.001 70.642 25.106 1.00 40.50 1289 CA PHE A 503 18.173 71.411 24.692 1.00 33.81 1290 C PHE A 503 17.908 72.827 24.212 1.00 28.39 1291 O PHE A 503 16.789 73.192 23.856 1.00 26.35 1292 CB PHE A 503 18.938 70.681 23.583 1.00 35.09 1293 CC PHE A 503 19.452 69.337 23.981 1.00 34.16 1294 CD1 PHE A 503 18.630 68.219 23.926 1.00 35.05 1295 CD2 PHE A 503 20.755 69.189 24.430 1.00 35.90 1296 CE1 PHE A 503 19.099 66.967 24.317 1.00 36.00 1297 CE2 PHE A 503 21.238 67.944 24.826 1.00 40.04 1298 CZ PHE A 503 20.408 66.829 24.771 1.00 38.82 1299 N PHE A 504 18.967 73.625 24.216 1.00 26.16 1300 CA PHE A 504 18.891 74.988 23.731 1.00 25.00 1301 C PHE A 504 20.182 75.314 23.004 1.00 26.57 1302 O PHE A 504 21.221 74.708 23.267 1.00 26.73 1303 CB PHE A 504 18.640 75.984 24.858 1.00 22.46 1304 CG PHE A 504 19.834 76.270 25.718 1.00 27.70 1305 CU PHE A 504 20.674 77.340 25.433 1.00 28.94 1306 CD2 PHE A 504 20.083 75.514 26.857 1.00 31.34 1307 CE1 PHE A 504 21.743 77.662 26.273 1.00 30.08 1308 CE2 PHE A 504 21.151 75.828 27.704 1.00 32.65 1309 CZ PHE A 504 21.979 76.909 27.403 1.00 32.80 1310 N VAL A 505 20.091 76.270 22.085 1.00 23.68 1311 CA VAL A 505 21.211 76.705 21.286 1.00 24.67 1312 C VAL A 505 21.041 78.215 21.072 1.00 23.86 1313 O VAL A 505 19.928 78.725 21.049 1.00 21.24 1314 CB VAL A 505 21.208 75.926 19.939 1.00 27.95 1315 CG1 VAL A 505 20.134 76.464 19.020 1.00 25.61 1316 CG2 VAL A 505 22.558 75.957 19.314 1.00 33.51 1317 N PHE A 506 22.146 78.936 20.959 1.00 26.20 1318 CA PHE A 506 22.086 80.382 20.754 1.00 26.10 1319 C PHE A 506 22.846 80.745 19.479 1.00 24.83 1320 O PHE A 506 23.928 80.231 19.241 1.00 25.52 1321 CB PHE A 506 22.725 81.104 21.939 1.00 28.18 1322 CG PHE A 506 22.758 82.593 21.797 1.00 35.33 1323 CD1 PHE A 506 21.620 83.355 22.020 1.00 42.56 1324 CD2 PHE A 506 23.937 83.241 21.443 1.00 40.04 1325 CE1 PHE A 506 21.660 84.746 21.892 1.00 44.70 1326 CR2 PHE A 506 23.987 84.623 21.311 1.00 40.54 1327 CZ PHE A 506 22.851 85.377 21.536 1.00 42.12 1328 N SER A 507 22.290 81.639 18.673 1.00 24.69 1329 CA SER A 507 22.941 82.050 17.426 1.00 24.73 1330 C SER A 507 23.065 83.578 17.355 1.00 26.40 1331 O SER A 507 22.113 84.292 17.609 1.00 25.99 1332 CB SER A 507 22.151 81.521 16.221 1.00 22.19 1333 OG SER A 507 22.740 81.947 15.009 1.00 30.30 1334 N ARG A 508 24.255 84.062 17.009 1.00 26.98 1335 CA ARG A 508 24.545 85.496 16.913 1.00 25.95 1336 C ARG A 508 24.851 85.911 15.463 1.00 24.97 1337 O ARG A 508 25.621 85.250 14.785 1.00 24.35 1338 CB ARG A 508 25.755 85.801 17.790 1.00 21.97 1339 CC ARG A 508 26.249 87.235 17.756 1.00 25.32 1340 CD ARG A 508 27.474 87.372 18.656 1.00 25.67 1341 NE ARG A 508 27.898 88.758 18.788 1.00 36.00 1342 CZ ARG A 508 28.757 89.357 17.972 1.00 36.06 1343 NH1 ARG A 508 29.293 88.682 16.963 1.00 34.19 1344 NH2 ARG A 508 29.062 90.633 18.157 1.00 34.70 1345 N LEU A 509 24.269 87.017 15.001 1.00 26.44 1346 CA LEU A 509 24.492 87.479 13.621 1.00 28.45 1347 C LEU A 509 24.794 88.973 13.540 1.00 28.87 1348 O LEU A 509 23.893 89.797 13.699 1.00 30.99 1349 CB LEU A 509 23.259 87.177 12.758 1.00 27.28 1350 CG LEU A 509 23.270 87.733 11.321 1.00 31.90 1351 CD1 LEU A 509 24.284 86.985 10.453 1.00 29.48 1352 CD2 LEU A 509 21.886 87.599 10.732 1.00 28.89 1353 N GLU A 510 26.054 89.323 13.288 1.00 31.92 1354 CA GLU A 510 26.448 90.728 13.189 1.00 34.67 1355 C GLU A 510 26.005 91.290 11.845 1.00 36.35 1356 O GLU A 510 26.199 90.652 10.812 1.00 34.66 1357 CB GLU A 510 27.970 90.875 13.343 1.00 41.07 1358 CG GLU A 510 28.510 90.383 14.696 1.00 54.35 1359 CD GLU A 510 29.997 90.675 14.911 1.00 58.86 1360 OE1 GLU A 510 30.811 90.364 14.013 1.00 61.22 1361 OE2 GLU A 510 30.349 91.207 15.989 1.00 61.34 1362 N VAL A 511 25.406 92.479 11.852 1.00 36.50 1363 CA VAL A 511 24.935 93.069 10.606 1.00 38.05 1364 C VAL A 511 25.370 94.516 10.408 1.00 42.41 1365 O VAL A 511 25.744 95.205 11.368 1.00 41.92 1366 CB VAL A 511 23.403 93.012 10.508 1.00 31.84 1367 CD1 VAL A 511 22.927 91.585 10.669 1.00 32.42 1368 CG2 VAL A 511 22.787 93.913 11.553 1.00 26.87 1369 N THR A 512 25.310 94.967 9.154 1.00 43.58 1370 CA THR A 512 25.697 96.331 8.808 1.00 48.37 1371 C THR A 512 24.602 97.306 9.201 1.00 50.53 1372 O THR A 512 23.487 96.894 9.516 1.00 51.77 1373 CB THR A 512 25.956 96.475 7.303 1.00 48.57 1374 OG1 THR A 512 24.766 96.140 6.581 1.00 46.96 1375 CG2 THR A 512 27.085 95.554 6.866 1.00 45.82 1376 N ARG A 513 24.922 98.598 9.188 1.00 53.29 1377 CA ARG A 513 23.952 99.629 9.544 1.00 55.54 1378 C ARG A 513 22.781 99.557 8.577 1.00 55.38 1379 O ARG A 513 21.623 99.741 8.962 1.00 55.22 1380 CB ARG A 513 24.594 101.018 9.464 1.00 59.23 1381 CG ARG A 513 23.999 102.037 10.428 1.00 65.98 1382 CD ARG A 513 22.519 102.274 10.184 1.00 74.12 1383 NE ARG A 513 21.858 102.827 11.365 1.00 80.97 1384 CZ ARG A 513 20.581 103.197 11.413 1.00 83.64 1385 NH1 ARG A 513 19.809 103.084 10.340 1.00 86.02 1386 NN2 ARG A 513 20.072 103.673 12.543 1.00 85.44 1387 N ALA A 514 23.099 99.285 7.317 1.00 55.03 1388 CA ALA A 514 22.096 99.186 6.268 1.00 55.46 1389 C ALA A 514 21.061 98.104 6.571 1.00 56.10 1390 O ALA A 514 19.866 98.390 6.674 1.00 56.61 1391 CB ALA A 514 22.775 98.908 4.927 1.00 54.05 1392 N GLU A 515 21.509 96.859 6.712 1.00 55.46 1393 CA GLU A 515 20.575 95.781 6.995 1.00 55.34 1394 C GLU A 515 19.949 95.951 8.371 1.00 54.83 1395 O GLU A 515 18.877 95.410 8.644 1.00 52.33 1396 CB GLU A 515 21.265 94.413 6.868 1.00 57.76 1397 CG GLU A 515 22.716 94.379 7.312 1.00 62.58 1398 CD GLU A 515 23.416 93.082 6.937 1.00 63.27 1399 OE1 GLU A 515 23.168 92.565 5.829 1.00 64.89 1400 OE2 GLU A 515 24.228 92.586 7.741 1.00 66.59 1401 N TRP A 516 20.608 96.716 9.234 1.00 55.79 1402 CA TRP A 516 20.072 96.956 10.566 1.00 57.81 1403 C TRP A 516 18.818 97.822 10.464 1.00 58.51 1404 O TRP A 516 17.988 97.822 11.374 1.00 57.71 1405 CB TRP A 516 21.101 97.649 11.466 1.00 61.48 1406 CG TRP A 516 20.738 97.544 12.913 1.00 66.54 1407 CD1 TRP A 516 20.823 96.428 13.697 1.00 67.26 1408 CD2 TRP A 516 20.140 98.561 13.725 1.00 69.56 1409 NE1 TRP A 516 20.309 96.685 14.946 1.00 71.76 1410 CE2 TRP A 516 19.882 97.987 14.990 1.00 70.88 1411 CE3 TRP A 516 19.793 99.900 13.507 1.00 70.94 1412 CZ2 TRP A 516 19.292 98.706 16.034 1.00 73.50 1413 CZ3 TRP A 516 19.204 100.618 14.548 1.00 74.37 1414 CH2 TRP A 516 18.961 100.016 15.796 1.00 74.71 1415 N GLU A 517 18.682 98.553 9.356 1.00 59.66 1416 CA GLU A 517 17.515 99.409 9.128 1.00 61.72 1417 C GLU A 517 16.301 98.565 8.746 1.00 59.87 1418 O GLU A 517 15.159 98.994 8.904 1.00 58.60 1419 CB GLU A 517 17.782 100.418 8.003 1.00 68.82 1420 CD GLU A 517 18.988 101.316 8.221 1.00 80.60 1421 CD GLU A 517 19.148 102.358 7.124 1.00 87.42 1422 GE1 GLU A 517 18.472 102.231 6.079 1.00 94.80 1423 OE2 GLU A 517 19.955 103.299 7.300 1.00 95.35 1424 N GLN A 518 16.555 97.366 8.233 1.00 57.92 1425 CA GLN A 518 15.480 96.468 7.836 1.00 55.74 1426 C GLN A 518 15.543 95.184 8.664 1.00 54.32 1427 O GLN A 518 15.207 94.102 8.176 1.00 52.85 1428 CB GLN A 518 15.600 96.146 6.355 1.00 54.10 1429 N LYS A 519 15.954 95.313 9.924 1.00 52.69 1430 CA LYS A 519 16.082 94.152 10.791 1.00 52.35 1431 C LYS A 519 14.781 93.394 10.941 1.00 51.69 1432 O LYS A 519 14.778 92.203 11.246 1.00 49.61 1433 CB LYS A 519 16.617 94.561 12.163 1.00 54.31 1434 CG LYS A 519 15.688 95.395 13.012 1.00 55.80 1435 CD LYS A 519 16.438 95.877 14.241 1.00 60.32 1436 CE LYS A 519 15.598 96.806 15.089 1.00 64.05 1437 NZ LYS A 519 16.409 97.377 16.202 1.00 70.92 1438 N ASP A 520 13.676 94.089 10.712 1.00 52.66 1439 CA ASP A 520 12.349 93.495 10.812 1.00 54.22 1440 C ASP A 520 12.204 92.391 9.764 1.00 53.07 1441 O ASP A 520 11.336 91.525 9.871 1.00 52.75 1442 CB ASP A 520 11.289 94.568 10.563 1.00 61.14 1443 CD ASP A 520 11.821 95.980 10.792 1.00 71.19 1444 OD1 ASP A 520 12.193 96.300 11.945 1.00 76.53 1445 OD2 ASP A 520 11.871 96.766 9.817 1.00 72.86 1446 N GLU A 521 13.067 92.423 8.757 1.00 51.01 1447 CA GLU A 521 13.018 91.443 7.684 1.00 50.49 1448 C GLU A 521 13.886 90.206 7.899 1.00 47.73 1449 O GLU A 521 13.762 89.228 7.165 1.00 48.58 1450 CB GLU A 521 13.400 92.107 6.362 1.00 53.54 1451 CG GLU A 521 12.423 93.173 5.901 1.00 60.11 1452 CD GLU A 521 12.901 93.895 4.658 1.00 65.41 1453 GE1 GLU A 521 13.103 93.239 3.614 1.00 67.98 1454 OE2 GLU A 521 13.079 95.129 4.726 1.00 73.58 1455 N PHE A 522 14.772 90.241 8.887 1.00 42.66 1456 CA PHE A 522 15.615 89.081 9.137 1.00 38.90 1457 C PHE A 522 14.847 88.017 9.892 1.00 35.93 1458 O PHE A 522 14.021 88.324 10.755 1.00 38.85 1459 CB PHE A 522 16.884 89.478 9.886 1.00 36.56 1460 CG PHE A 522 17.890 90.181 9.019 1.00 39.04 1461 CD1 PHE A 522 17.673 91.494 8.605 1.00 42.28 1462 CD2 PHE A 522 19.026 89.513 8.561 1.00 36.78 1463 CE1 PHE A 522 18.571 92.132 7.738 1.00 44.30 1464 CE2 PHE A 522 19.927 90.139 7.695 1.00 40.92 1465 CZ PHE A 522 19.699 91.454 7.283 1.00 39.51 1466 N ILE A 523 15.108 86.763 9.545 1.00 31.27 1467 CA ILE A 523 14.427 85.641 10.156 1.00 29.65 1468 C ILE A 523 15.389 84.551 10.617 1.00 29.13 1469 O ILE A 523 16.364 84.240 9.936 1.00 27.36 1470 CB ILE A 523 13.420 85.033 9.163 1.00 34.21 1471 CG1 ILE A 523 12.349 86.072 8.818 1.00 37.38 1472 CC2 ILE A 523 12.804 83.773 9.736 1.00 34.94 1473 CD1 ILE A 523 11.373 85.619 7.746 1.00 38.56 1474 N CYS A 524 15.102 83.990 11.789 1.00 26.34 1475 CA CYS A 524 15.901 82.914 12.361 1.00 27.10 1476 C CYS A 524 15.100 81.654 12.138 1.00 26.67 1477 O CYS A 524 13.945 81.590 12.531 1.00 27.58 1478 CB CYS A 524 16.103 83.127 13.874 1.00 24.27 1479 SG CYS A 524 16.974 81.777 14.737 1.00 37.60 1480 N ARG A 525 15.714 80.649 11.528 1.00 26.37 1481 CA ARG A 525 15.024 79.406 11.244 1.00 26.35 1482 C ARG A 525 15.713 78.181 11.796 1.00 26.72 1483 O ARG A 525 16.929 78.039 11.700 1.00 29.04 1484 CB ARG A 525 14.852 79.224 9.739 1.00 29.81 1485 CG ARG A 525 14.207 77.887 9.372 1.00 35.40 1486 CD ARG A 525 13.542 77.948 8.001 1.00 46.51 1487 NE ARG A 525 14.487 77.804 6.907 1.00 50.77 1488 CZ ARG A 525 14.221 78.139 5.649 1.00 55.09 1489 NH1 ARG A 525 13.035 78.649 5.337 1.00 54.58 1490 NH2 ARG A 525 15.136 77.950 4.703 1.00 56.77 1491 N ALA A 526 14.920 77.289 12.369 1.00 25.38 1492 CA ALA A 526 15.458 76.072 12.920 1.00 25.38 1493 C ALA A 526 14.872 74.879 12.175 1.00 25.99 1494 O ALA A 526 13.667 74.849 11.890 1.00 25.50 1495 CB ALA A 526 15.116 75.971 14.404 1.00 25.98 1496 N VAL A 527 15.728 73.916 11.841 1.00 23.84 1497 CA VAL A 527 15.267 72.705 11.198 1.00 25.15 1498 C VAL A 527 15.522 71.628 12.220 1.00 26.30 1499 O VAL A 527 16.642 71.481 12.706 1.00 26.20 1500 CB VAL A 527 16.043 72.365 9.923 1.00 24.43 1501 CG1 VAL A 527 15.610 71.012 9.439 1.00 26.95 1502 CG2 VAL A 527 15.781 73.409 8.849 1.00 28.13 1503 N HIS A 528 14.485 70.862 12.531 1.00 26.24 1504 CA HIS A 528 14.582 69.828 13.536 1.00 29.14 1505 C HIS A 528 13.498 68.778 13.295 1.00 31.86 1506 O HIS A 528 12.384 69.091 12.861 1.00 31.05 1507 CB HIS A 528 14.428 70.479 14.921 1.00 29.03 1508 CC HIS A 528 14.518 69.523 16.065 1.00 29.34 1509 ND1 HIS A 528 13.491 68.666 16.404 1.00 33.33 1510 CD2 HIS A 528 15.510 69.283 16.956 1.00 28.93 1511 CE1 HIS A 528 13.845 67.945 17.449 1.00 26.07 1512 NE2 HIS A 528 15.070 68.298 17.805 1.00 32.19 1513 N GLU A 529 13.843 67.536 13.599 1.00 34.08 1514 CA GLU A 529 12.964 66.393 13.424 1.00 39.76 1515 C GLU A 529 11.563 66.490 14.034 1.00 41.50 1516 O GLU A 529 10.580 66.190 13.360 1.00 41.48 1517 CB GLU A 529 13.641 65.138 13.978 1.00 43.03 1518 CG GLU A 529 12.702 63.935 14.014 1.00 56.19 1519 CD GLU A 529 13.239 62.773 14.826 1.00 62.66 1520 OE1 GLU A 529 12.489 61.788 15.007 1.00 63.52 1521 OE2 GLU A 529 14.402 62.842 15.281 1.00 65.43 1522 N ALA A 530 11.479 66.897 15.300 1.00 42.51 1523 CA ALA A 530 10.201 66.978 16.006 1.00 46.03 1524 C ALA A 530 9.269 68.105 15.596 1.00 49.29 1525 O ALA A 530 8.124 68.153 16.044 1.00 50.87 1526 CB ALA A 530 10.443 67.043 17.513 1.00 39.71 1527 N ALA A 531 9.751 69.005 14.748 1.00 52.89 1528 CA ALA A 531 8.949 70.133 14.302 1.00 56.14 1529 C ALA A 531 8.030 69.799 13.124 1.00 59.66 1530 O ALA A 531 8.258 70.243 12.004 1.00 61.00 1531 CB ALA A 531 9.864 71.295 13.938 1.00 52.83 1532 N SER A 532 6.992 69.012 13.370 1.00 63.07 1533 CA SER A 532 6.056 68.673 12.305 1.00 66.03 1534 C SER A 532 5.006 69.778 12.250 1.00 66.08 1535 O SER A 532 4.569 70.283 13.286 1.00 65.35 1536 CB SER A 532 5.384 67.330 12.593 1.00 68.98 1537 OG SER A 532 4.526 67.416 13.716 1.00 74.64 1538 N PRO A 533 4.581 70.173 11.043 1.00 66.51 1539 CA PRO A 533 4.931 69.713 9.696 1.00 65.99 1540 C PRO A 533 6.251 70.226 9.117 1.00 63.48 1541 O PRO A 533 6.760 71.273 9.518 1.00 64.33 1542 CD PRO A 533 3.757 70.203 8.873 1.00 69.06 1543 CG PRO A 533 3.539 71.556 9.471 1.00 71.08 1544 CD PRO A 533 3.570 71.242 10.963 1.00 70.23 1545 N SER A 534 6.783 69.466 8.165 1.00 59.21 1546 CA SER A 534 8.009 69.804 7.452 1.00 55.01 1547 C SER A 534 9.274 70.148 8.248 1.00 50.27 1548 O SER A 534 10.130 70.875 7.753 1.00 48.58 1549 CD SER A 534 7.706 70.934 6.475 1.00 58.20 1550 OG SER A 534 7.074 72.013 7.138 1.00 63.36 1551 N GLN A 535 9.387 69.616 9.461 1.00 44.89 1552 CA GLN A 535 10.543 69.829 10.330 1.00 42.88 1553 C GLN A 535 11.194 71.205 10.277 1.00 41.55 1554 O GLN A 535 12.419 71.321 10.294 1.00 40.80 1555 CB GLN A 535 11.633 68.769 10.080 1.00 37.08 1556 CG GLN A 535 11.302 67.731 9.056 1.00 47.40 1557 CD GLN A 535 10.101 66.916 9.431 1.00 44.36 1558 OE1 GLN A 535 9.193 66.738 8.625 1.00 47.59 1559 NE2 GLN A 535 10.079 66.415 10.664 1.00 54.70 1560 N THR A 536 10.387 72.252 10.226 1.00 39.97 1561 CA THR A 536 10.950 73.588 10.207 1.00 40.62 1562 C THR A 536 10.113 74.575 11.023 1.00 37.57 1563 O THR A 536 8.893 74.558 10.975 1.00 40.85 1564 CB THR A 536 11.137 74.092 8.747 1.00 42.38 1565 OG1 THR A 536 11.458 75.488 8.763 1.00 44.59 1566 CG2 THR A 536 9.881 73.870 7.932 1.00 49.65 1567 N VAL A 537 10.788 75.410 11.801 1.00 35.29 1568 CA VAL A 537 10.147 76.418 12.632 1.00 31.25 1569 C VAL A 537 10.996 77.678 12.537 1.00 29.01 1570 O VAL A 537 12.218 77.615 12.699 1.00 30.11 1571 CB VAL A 537 10.106 75.996 14.117 1.00 34.80 1572 CG1 VAL A 537 9.452 77.084 14.939 1.00 35.52 1573 CG2 VAL A 537 9.341 74.712 14.278 1.00 37.19 1574 N GLN A 538 10.365 78.820 12.292 1.00 26.73 1575 CA GLN A 538 11.107 80.067 12.167 1.00 26.74 1576 C GLN A 538 10.376 81.271 12.732 1.00 27.53 1577 O CLN A 538 9.169 81.249 12.902 1.00 29.89 1578 CB GLN A 538 11.424 80.335 10.700 1.00 28.48 1579 CG GLN A 538 10.208 80.624 9.834 1.00 25.88 1580 CD GLN A 538 10.595 80.853 8.378 1.00 28.51 1581 OE1 CLN A 538 11.390 80.102 7.810 1.00 31.66 1582 NE2 GLN A 538 10.035 81.885 7.772 1.00 27.39 1583 N ARG A 539 11.113 82.334 13.013 1.00 28.05 1584 CA ARG A 539 10.493 83.530 13.535 1.00 30.72 1585 C ARG A 539 11.288 84.742 13.114 1.00 31.33 1586 O ARG A 539 12.517 84.703 13.077 1.00 32.42 1587 CB ARG A 539 10.420 83.463 15.061 1.00 36.30 1588 CG ARG A 539 9.488 84.476 15.686 1.00 45.60 1589 CD ARG A 539 8.741 83.829 16.830 1.00 57.97 1590 NE ARG A 539 8.118 82.591 16.371 1.00 69.46 1591 CZ ARG A 539 7.453 81.745 17.150 1.00 78.18 1592 NH1 ARG A 539 7.316 81.996 18.447 1.00 83.01 1593 NH2 ARG A 539 6.927 80.641 16.630 1.00 81.89 1594 N ALA A 540 10.578 85.818 12.799 1.00 31.92 1595 CA ALA A 540 11.207 87.054 12.383 1.00 34.50 1596 C ALA A 540 11.691 87.774 13.634 1.00 36.68 1597 O ALA A 540 11.190 87.532 14.739 1.00 34.62 1598 CB ALA A 540 10.209 87.907 11.621 1.00 33.91 1599 N VAL A 541 12.694 88.626 13.460 1.00 39.73 1600 CA VAL A 541 13.254 89.386 14.572 1.00 44.47 1601 C VAL A 541 12.164 90.249 15.218 1.00 46.91 1602 O VAL A 541 11.595 91.124 14.573 1.00 44.53 1603 CB VAL A 541 14.415 90.295 14.090 1.00 42.49 1604 CC1 VAL A 541 14.715 91.358 15.130 1.00 47.96 1605 CC2 VAL A 541 15.655 89.460 13.831 1.00 42.43 1606 N SER A 542 11.869 89.997 16.489 1.00 52.25 1607 CA SER A 542 10.840 90.771 17.174 1.00 60.05 1608 C SER A 542 11.374 92.174 17.421 1.00 64.25 1609 O SER A 542 12.550 92.353 17.743 1.00 65.22 1610 CB SER A 542 10.443 90.110 18.500 1.00 60.43 1611 DC SER A 542 11.530 90.076 19.404 1.00 65.30 1612 N VAL A 543 10.510 93.168 17.256 1.00 68.19 1613 CA VAL A 543 10.906 94.557 17.444 1.00 72.45 1614 C VAL A 543 9.828 95.323 18.202 1.00 74.32 1615 O VAL A 543 8.970 95.979 17.603 1.00 75.99 1616 CB VAL A 543 11.148 95.247 16.084 1.00 74.41 1617 CC1 VAL A 543 11.530 96.705 16.299 1.00 76.37 1618 CC2 VAL A 543 12.233 94.514 15.318 1.00 75.78 1619 N VAL B 336 42.982 59.443 29.109 1.00 58.93 1620 CA VAL B 336 43.788 60.200 30.107 1.00 60.44 1621 C VAL B 336 44.173 61.587 29.599 1.00 60.07 1622 O VAL B 336 45.211 61.753 28.958 1.00 61.48 1623 CB VAL B 336 45.079 59.445 30.453 1.00 60.81 1624 CC1 VAL B 336 45.794 60.136 31.600 1.00 61.71 1625 CC2 VAL B 336 44.755 58.010 30.798 1.00 64.73 1626 N SER B 337 43.343 62.583 29.891 1.00 57.95 1627 CA SER B 337 43.617 63.945 29.452 1.00 56.60 1628 C SER B 337 43.758 64.917 30.624 1.00 55.17 1629 O SER B 337 43.338 64.619 31.748 1.00 54.55 1630 CB SER B 337 42.522 64.415 28.497 1.00 57.92 1631 DC SER B 337 41.244 64.111 29.013 1.00 64.70 1632 N ALA B 338 44.362 66.073 30.357 1.00 52.40 1633 CA ALA B 338 44.590 67.078 31.389 1.00 50.69 1634 C ALA B 338 44.300 68.491 30.908 1.00 50.25 1635 O ALA B 338 44.538 68.828 29.746 1.00 51.17 1636 CB ALA B 338 46.027 66.989 31.889 1.00 50.21 1637 N TYR B 339 43.792 69.319 31.816 1.00 48.22 1638 CA TYR B 339 43.461 70.701 31.495 1.00 46.82 1639 C TYR B 339 43.834 71.610 32.669 1.00 44.51 1640 O TYR B 339 43.711 71.228 33.832 1.00 42.27 1641 CB TYR B 339 41.962 70.835 31.185 1.00 50.52 1642 CG TYR B 339 41.402 69.731 30.307 1.00 58.40 1643 CD1 TYR B 339 41.155 68.456 30.826 1.00 61.23 1644 CD2 TYR B 339 41.144 69.952 28.949 1.00 60.99 1645 CE1 TYR B 339 40.671 67.426 30.019 1.00 62.71 1646 CE2 TYR B 339 40.657 68.926 28.131 1.00 63.53 1647 CZ TYR B 339 40.424 67.667 28.673 1.00 64.33 1648 OH TYR B 339 39.956 66.647 27.870 1.00 65.07 1649 N LEU B 340 44.309 72.807 32.354 1.00 41.90 1650 CA LEU B 340 44.695 73.769 33.372 1.00 41.06 1651 C LEU B 340 43.929 75.029 33.022 1.00 41.10 1652 O LEU B 340 43.953 75.464 31.876 1.00 43.45 1653 CB LEU B 340 46.208 74.017 33.321 1.00 36.93 1654 CG LEU B 340 46.830 74.911 34.399 1.00 35.91 1655 CD1 LEU B 340 46.500 74.371 35.786 1.00 34.60 1656 CD2 LEU B 340 48.336 74.979 34.194 1.00 35.51 1657 N SER B 341 43.232 75.610 33.992 1.00 39.82 1658 CA SER B 341 42.448 76.810 33.715 1.00 39.85 1659 C SER B 341 42.955 78.002 34.486 1.00 37.88 1660 O SER B 341 43.524 77.863 35.556 1.00 42.10 1661 CB SER B 341 40.973 76.575 34.058 1.00 39.34 1662 OG SER B 341 40.808 76.253 35.428 1.00 44.58 1663 N ARG B 342 42.732 79.185 33.942 1.00 36.98 1664 CA ARG B 342 43.163 80.413 34.583 1.00 35.20 1665 C ARG B 342 42.183 80.747 35.707 1.00 33.18 1666 O ARG B 342 41.157 80.092 35.848 1.00 33.16 1667 CB ARG B 342 43.206 81.530 33.534 1.00 38.57 1668 CC ARG B 342 44.219 81.279 32.411 1.00 39.10 1669 CD ARG B 342 44.236 82.409 31.388 1.00 43.21 1670 NE ARG B 342 43.056 82.369 30.530 1.00 45.40 1671 CZ ARG B 342 42.886 81.514 29.527 1.00 48.22 1672 NH1 ARG B 342 43.823 80.623 29.240 1.00 52.78 1673 NH2 ARG B 342 41.769 81.541 28.814 1.00 54.34 1674 N PRO B 343 42.488 81.757 36.530 1.00 33.03 1675 CA PRO B 343 41.560 82.103 37.619 1.00 34.14 1676 C PRO B 343 40.261 82.693 37.065 1.00 34.06 1677 O PRO B 343 40.259 83.298 35.994 1.00 35.44 1678 CB PRO B 343 42.334 83.152 38.433 1.00 33.07 1679 CC PRO B 343 43.789 82.900 38.075 1.00 35.06 1680 CD PRO B 343 43.715 82.571 36.601 1.00 33.27 1681 N SER B 344 39.155 82.520 37.775 1.00 32.17 1682 CA SER B 344 37.909 83.110 37.308 1.00 31.75 1683 C SER B 344 37.983 84.586 37.686 1.00 32.07 1684 O SER B 344 38.485 84.940 38.756 1.00 30.21 1685 CB SER B 344 36.693 82.456 37.982 1.00 32.20 1686 OC SER B 344 36.487 82.935 39.301 1.00 32.50 1687 N PRO B 345 37.512 85.473 36.800 1.00 32.31 1688 CA PRO B 345 37.561 86.899 37.125 1.00 30.84 1689 C PRO B 345 36.890 87.219 38.471 1.00 29.64 1690 O PRO B 345 37.344 88.094 39.209 1.00 30.14 1691 CB PRO B 345 36.859 87.545 35.926 1.00 30.96 1692 CC PRO B 345 37.299 86.659 34.793 1.00 33.18 1693 CD PRO B 345 37.143 85.261 35.387 1.00 33.65 1694 N PHE B 346 35.831 86.497 38.808 1.00 28.34 1695 CA PHE B 346 35.153 86.756 40.066 1.00 31.46 1696 C PHE B 346 36.078 86.515 41.269 1.00 32.46 1697 O PHE B 346 36.135 87.331 42.193 1.00 32.59 1698 CB PHE B 346 33.894 85.889 40.184 1.00 32.72 1699 CC PHE B 346 33.218 85.987 41.521 1.00 36.34 1700 CD1 PHE B 346 32.619 87.170 41.928 1.00 40.58 1701 CD2 PHE B 346 33.189 84.898 42.378 1.00 36.76 1702 CE1 PHE B 346 31.991 87.267 43.167 1.00 38.98 1703 CR2 PHE B 346 32.563 84.985 43.618 1.00 40.15 1704 CZ PHE B 346 31.963 86.175 44.014 1.00 38.60 1705 N ASP B 347 36.803 85.397 41.250 1.00 32.92 1706 CA ASP B 347 37.723 85.066 42.336 1.00 33.58 1707 C ASP B 347 38.896 86.045 42.367 1.00 34.26 1708 O ASP B 347 39.388 86.408 43.434 1.00 32.29 1709 CB ASP B 347 38.251 83.633 42.179 1.00 28.72 1710 CG ASP B 347 37.236 82.592 42.579 1.00 39.62 1711 OD1 ASP B 347 37.515 81.375 42.429 1.00 42.08 1712 OD2 ASP B 347 36.151 82.991 43.054 1.00 46.23 1713 N LEU B 348 39.324 86.480 41.189 1.00 34.31 1714 CA LEU B 348 40.441 87.403 41.064 1.00 37.70 1715 C LEU B 348 40.159 88.858 41.471 1.00 38.98 1716 O LEU B 348 40.949 89.463 42.198 1.00 38.11 1717 CB LEU B 348 40.959 87.380 39.618 1.00 40.66 1718 CG LEU B 348 42.159 88.267 39.260 1.00 41.99 1719 CD1 LEU B 348 43.388 87.862 40.095 1.00 42.77 1720 CD2 LEU B 348 42.469 88.124 37.759 1.00 41.00 1721 N PHE B 349 39.040 89.417 41.017 1.00 39.68 1722 CA PHE B 349 38.725 90.819 41.306 1.00 42.09 1723 C PHE B 349 37.717 91.134 42.405 1.00 45.09 1724 O PHE B 349 37.821 92.169 43.062 1.00 48.27 1725 CB PHE B 349 38.272 91.526 40.029 1.00 37.36 1726 CC PHE B 349 39.244 91.411 38.900 1.00 36.93 1727 CD1 PHE B 349 38.976 90.579 37.818 1.00 38.16 1728 CD2 PHE B 349 40.444 92.113 38.926 1.00 38.04 1729 CE1 PHE B 349 39.885 90.445 36.781 1.00 38.11 1730 CE2 PHE B 349 41.369 91.986 37.887 1.00 37.58 1731 CZ PHE B 349 41.089 91.151 36.817 1.00 40.39 1732 N ILE B 350 36.726 90.277 42.600 1.00 46.66 1733 CA ILE B 350 35.746 90.548 43.639 1.00 48.94 1734 C ILE B 350 36.200 89.905 44.950 1.00 51.15 1735 O ILE B 350 36.505 90.593 45.921 1.00 50.51 1736 CB ILE B 350 34.359 90.008 43.240 1.00 48.52 1737 CG1 ILE B 350 34.038 90.428 41.801 1.00 49.25 1738 CG2 ILE B 350 33.300 90.548 44.177 1.00 49.68 1739 CD1 ILE B 350 34.242 91.911 41.533 1.00 46.80 1740 N ARG B 351 36.265 88.579 44.945 1.00 52.64 1741 CA ARG B 351 36.669 87.793 46.100 1.00 53.76 1742 C ARG B 351 38.114 88.090 46.519 1.00 53.61 1743 O ARG B 351 38.436 88.094 47.703 1.00 53.55 1744 CB ARG B 351 36.505 86.313 45.759 1.00 56.64 1745 CG ARG B 351 36.016 85.434 46.894 1.00 62.18 1746 CD ARG B 351 35.073 84.375 46.348 1.00 66.96 1747 NE ARG B 351 34.958 83.211 47.219 1.00 71.13 1748 CZ ARG B 351 35.957 82.371 47.470 1.00 76.72 1749 NH1 ARG B 351 37.145 82.573 46.916 1.00 78.73 1750 NE2 ARG B 351 35.771 81.325 48.268 1.00 77.63 1751 N LYS B 352 38.974 88.347 45.540 1.00 53.86 1752 CA LYS B 352 40.385 88.646 45.788 1.00 54.12 1753 C LYS B 352 41.172 87.449 46.328 1.00 52.02 1754 O LYS B 352 42.078 87.604 47.146 1.00 51.77 1755 CB LYS B 352 40.525 89.825 46.753 1.00 57.77 1756 CG LYS B 352 39.911 91.124 46.254 1.00 62.15 1757 CD LYS B 352 40.161 92.252 47.254 1.00 71.06 1758 CE LYS B 352 39.351 93.502 46.929 1.00 74.25 1759 NZ LYS B 352 37.893 93.307 47.185 1.00 78.35 1760 N SER B 353 40.811 86.258 45.867 1.00 48.01 1761 CA SER B 353 41.488 85.032 46.268 1.00 45.29 1762 C SER B 353 41.446 84.056 45.084 1.00 40.67 1763 O SER B 353 40.725 83.054 45.106 1.00 40.76 1764 CB SER B 353 40.809 84.423 47.498 1.00 47.97 1765 OG SER B 353 39.445 84.152 47.247 1.00 56.20 1766 N PRO B 354 42.225 84.356 44.030 1.00 36.53 1767 CA PRO B 354 42.361 83.596 42.781 1.00 32.68 1768 C PRO B 354 42.940 82.201 42.961 1.00 31.88 1769 O PRO B 354 43.813 81.985 43.798 1.00 29.76 1770 CB PRO B 354 43.306 84.453 41.940 1.00 30.29 1771 CG PRO B 354 43.260 85.801 42.587 1.00 41.68 1772 CD PRO B 354 43.155 85.494 44.035 1.00 33.29 1773 N THR B 355 42.446 81.258 42.168 1.00 30.03 1774 CA THR B 355 42.956 79.896 42.198 1.00 29.70 1775 C THR B 355 43.022 79.364 40.774 1.00 30.82 1776 O THR B 355 42.302 79.827 39.887 1.00 30.67 1777 CB TNR B 355 42.042 78.931 42.964 1.00 32.14 1778 OG1 THR B 355 40.815 78.794 42.240 1.00 29.97 1779 CG2 THR B 355 41.763 79.425 44.393 1.00 31.76 1780 N ILE B 356 43.907 78.405 40.542 1.00 30.53 1781 CA ILE B 356 43.969 77.784 39.232 1.00 31.56 1782 C ILE B 356 43.740 76.321 39.525 1.00 31.79 1783 O ILE B 356 44.039 75.848 40.625 1.00 30.35 1784 CB ILE B 356 45.315 78.016 38.517 1.00 30.05 1785 CG1 ILE B 356 46.467 77.499 39.371 1.00 31.32 1786 CG2 ILE B 356 45.469 79.508 38.210 1.00 31.27 1787 CD1 ILE B 356 47.828 77.757 38.763 1.00 36.89 1788 N THR B 357 43.198 75.605 38.550 1.00 33.31 1789 CA THR B 357 42.881 74.205 38.751 1.00 33.68 1790 C THR B 357 43.403 73.318 37.644 1.00 35.47 1791 O THR B 357 43.228 73.607 36.459 1.00 36.65 1792 CB THR B 357 41.335 74.011 38.855 1.00 33.81 1793 OG1 THR B 357 40.844 74.683 40.023 1.00 33.71 1794 CG2 THR B 357 40.968 72.535 38.921 1.00 29.63 1795 N CYS B 358 44.034 72.228 38.048 1.00 35.41 1796 CA CYS B 358 44.561 71.254 37.110 1.00 38.12 1797 C CYS B 358 43.570 70.093 37.165 1.00 37.77 1798 O CYS B 358 43.395 69.473 38.210 1.00 36.67 1799 CB CYS B 358 45.945 70.789 37.568 1.00 40.37 1800 SG CYS B 358 46.871 69.769 36.374 1.00 49.83 1801 N LEU B 359 42.909 69.822 36.046 1.00 39.77 1802 CA LEU B 359 41.932 68.747 35.973 1.00 42.86 1803 C LEU B 359 42.432 67.593 35.123 1.00 46.01 1804 O LEU B 359 42.748 67.769 33.948 1.00 47.43 1805 CB LEU B 359 40.612 69.265 35.389 1.00 42.74 1806 CC LEU B 359 39.604 68.208 34.904 1.00 45.03 1807 CD1 LEU B 359 39.152 67.338 36.057 1.00 47.59 1808 CD2 LEU B 359 38.403 68.889 34.262 1.00 47.51 1809 N VAL B 360 42.493 66.411 35.721 1.00 48.26 1810 CA VAL B 360 42.931 65.220 35.010 1.00 52.34 1811 C VAL B 360 41.765 64.243 34.883 1.00 55.48 1812 O VAL B 360 41.092 63.928 35.866 1.00 55.57 1813 CB VAL B 360 44.100 64.527 35.747 1.00 53.36 1814 CG1 VAL B 360 44.481 63.240 35.029 1.00 51.62 1815 CG2 VAL B 360 45.299 65.467 35.816 1.00 51.77 1816 N VAL B 361 41.520 63.773 33.665 1.00 58.92 1817 CA VAL B 361 40.433 62.834 33.416 1.00 63.13 1818 C VAL B 361 40.993 61.506 32.926 1.00 67.77 1819 O VAL B 361 41.738 61.466 31.946 1.00 68.38 1820 CB VAL B 361 39.442 63.377 32.353 1.00 60.50 1821 CG1 VAL B 361 38.358 62.355 32.086 1.00 56.92 1822 CG2 VAL B 361 38.814 64.671 32.830 1.00 56.10 1823 N ASP B 362 40.635 60.426 33.615 1.00 72.90 1824 CA ASP B 362 41.098 59.085 33.259 1.00 78.30 1825 C ASP B 362 39.904 58.244 32.816 1.00 81.68 1826 O ASP B 362 39.168 57.709 33.648 1.00 81.72 1827 CB ASP B 362 41.771 58.415 34.462 1.00 80.22 1828 CG ASP B 362 42.530 57.156 34.080 1.00 84.67 1829 OD1 ASP B 362 42.113 56.478 33.117 1.00 87.54 1830 OD2 ASP B 362 43.537 56.837 34.749 1.00 87.19 1831 N LEU B 363 39.723 58.126 31.503 1.00 85.84 1832 CA LEU B 363 38.614 57.366 30.935 1.00 89.95 1833 C LEU B 363 38.562 55.923 31.428 1.00 92.20 1834 O LEU B 363 37.483 55.386 31.668 1.00 92.55 1835 CB LEU B 363 38.694 57.390 29.409 1.00 91.66 1836 CG LEU B 363 38.719 58.777 28.758 1.00 92.93 1837 CD1 LEU B 363 38.813 58.624 27.246 1.00 95.41 1838 CD2 LEU B 363 37.471 59.551 29.137 1.00 92.73 1839 N ALA B 364 39.726 55.296 31.573 1.00 94.76 1840 CA ALA B 364 39.801 53.916 32.051 1.00 97.66 1841 C ALA B 364 40.794 53.831 33.210 1.00 99.72 1842 O ALA B 364 41.998 53.996 33.021 1.00 100.44 1843 CB ALA B 364 40.235 52.996 30.921 1.00 97.99 1844 N PRO B 365 40.297 53.577 34.429 1.00 101.15 1845 CA PRO B 365 41.173 53.484 35.602 1.00 102.25 1846 C PRO B 365 41.895 52.163 35.855 1.00 103.43 1847 O PRO B 365 41.274 51.103 35.934 1.00 104.19 1848 CB PRO B 365 40.237 53.829 36.761 1.00 101.91 1849 CC PRO B 365 39.121 54.617 36.098 1.00 102.27 1850 CD PRO B 365 38.910 53.833 34.846 1.00 101.40 1851 N SER B 366 43.215 52.256 35.979 1.00 104.18 1852 CA SER B 366 44.088 51.132 36.299 1.00 104.43 1853 C SER B 366 44.573 51.676 37.637 1.00 104.05 1854 O SER B 366 44.888 52.864 37.727 1.00 104.36 1855 CB SER B 366 45.249 51.055 35.312 1.00 105.50 1856 OG SER B 366 46.040 52.223 35.413 1.00 106.70 1857 N LYS B 367 44.645 50.861 38.682 1.00 103.19 1858 CA LYS B 367 45.041 51.462 39.944 1.00 102.08 1859 C LYS B 367 46.491 51.630 40.367 1.00 100.74 1860 O LYS B 367 47.234 50.683 40.640 1.00 101.05 1861 CB LYS B 367 44.236 50.868 41.102 1.00 103.30 1862 CC LYS B 367 44.343 49.384 41.345 1.00 105.00 1863 CD LYS B 367 43.374 49.046 42.467 1.00 104.80 1864 CE LYS B 367 43.467 47.610 42.930 1.00 104.70 1865 NZ LYS B 367 42.524 47.386 44.066 1.00 105.18 1866 N CLY B 368 46.839 52.909 40.422 1.00 98.70 1867 CA GLY B 368 48.136 53.408 40.828 1.00 95.62 1868 C GLY B 368 47.700 54.801 41.244 1.00 93.12 1869 O GLY B 368 46.538 55.143 41.035 1.00 93.17 1870 N THR B 369 48.569 55.617 41.823 1.00 90.15 1871 CA THR B 369 48.125 56.948 42.220 1.00 86.41 1872 C THR B 369 48.420 57.977 41.136 1.00 83.04 1873 O THR B 369 49.402 57.854 40.401 1.00 82.54 1874 CB THR B 369 48.792 57.397 43.541 1.00 87.73 1875 OG1 THR B 369 50.217 57.422 43.379 1.00 88.60 1876 CG2 THR B 369 48.423 56.443 44.671 1.00 86.64 1877 N VAL B 370 47.552 58.980 41.027 1.00 79.07 1878 CA VAL B 370 47.729 60.041 40.042 1.00 74.46 1879 C VAL B 370 48.275 61.261 40.768 1.00 72.21 1880 O VAL B 370 47.602 61.838 41.618 1.00 71.35 1881 CB VAL B 370 46.401 60.420 39.368 1.00 73.33 1882 CD1 VAL B 370 46.667 61.346 38.196 1.00 70.92 1883 CG2 VAL B 370 45.674 59.173 38.915 1.00 69.77 1884 N ASN B 371 49.498 61.653 40.426 1.00 70.13 1885 CA ASN B 371 50.137 62.791 41.073 1.00 68.15 1886 C ASN B 371 50.157 64.079 40.262 1.00 65.65 1887 O ASN B 371 50.352 64.067 39.046 1.00 64.64 1888 CB ASN B 371 51.564 62.421 41.469 1.00 70.12 1889 CG ASN B 371 51.605 61.330 42.508 1.00 73.56 1890 OD1 ASN B 371 51.153 61.519 43.638 1.00 75.10 1891 ND2 ASN B 371 52.137 60.173 42.131 1.00 74.76 1892 N LEU B 372 49.949 65.192 40.959 1.00 62.66 1893 CA LEU B 372 49.959 66.512 40.346 1.00 59.53 1894 C LEU B 372 50.927 67.374 41.137 1.00 56.68 1895 O LEU B 372 50.788 67.529 42.347 1.00 56.70 1896 CB LEU B 372 48.560 67.141 40.372 1.00 59.44 1897 CG LEU B 372 47.428 66.383 39.678 1.00 60.55 1898 CU LEU B 372 46.214 67.277 39.579 1.00 61.28 1899 CD2 LEU B 372 47.861 65.956 38.293 1.00 62.83 1900 N THR B 373 51.911 67.931 40.446 1.00 53.76 1901 CA THR B 373 52.915 68.766 41.085 1.00 51.64 1902 C THR B 373 52.850 70.180 40.512 1.00 48.20 1903 O THR B 373 52.801 70.355 39.296 1.00 46.65 1904 CB THR B 373 54.325 68.201 40.832 1.00 53.15 1905 CG1 THR B 373 54.324 66.789 41.073 1.00 57.77 1906 CG2 THR B 373 55.339 68.871 41.747 1.00 53.75 1907 N TRP B 374 52.851 71.181 41.385 1.00 45.34 1908 CA TRP B 374 52.799 72.575 40.942 1.00 44.94 1909 C TRP B 374 54.161 73.259 41.041 1.00 43.68 1910 O TRP B 374 54.945 72.964 41.938 1.00 42.67 1911 CB TRP B 374 51.805 73.391 41.784 1.00 41.63 1912 CG TRP B 374 50.371 72.977 41.657 1.00 41.50 1913 CD1 TRP B 374 49.688 72.124 42.477 1.00 39.67 1914 CD2 TRP B 374 49.441 73.395 40.648 1.00 35.69 1915 NE1 TRP B 374 48.392 71.988 42.041 1.00 35.06 1916 CE2 TRP B 374 48.214 72.756 40.922 1.00 34.53 1917 CE3 TRP B 374 49.528 74.247 39.542 1.00 32.37 1918 CZ2 TRP B 374 47.079 72.943 40.129 1.00 35.43 1919 CZ3 TRP B 374 48.401 74.434 38.751 1.00 36.11 1920 CH2 TRP B 374 47.190 73.782 39.050 1.00 37.51 1921 N SER B 375 54.430 74.179 40.119 1.00 43.53 1922 CA SER B 375 55.678 74.934 40.140 1.00 43.57 1923 C SER B 375 55.511 76.270 39.438 1.00 42.59 1924 O SER B 375 54.669 76.411 38.550 1.00 43.68 1925 CB SER B 375 56.820 74.153 39.474 1.00 45.03 1926 OG SER B 375 56.691 74.118 38.066 1.00 45.66 1927 N ARG B 376 56.299 77.251 39.866 1.00 40.79 1928 CA ARG B 376 56.279 78.569 39.266 1.00 40.12 1929 C ARG B 376 57.498 78.689 38.351 1.00 40.59 1930 O ARG B 376 58.618 78.393 38.752 1.00 40.90 1931 CB ARG B 376 56.345 79.653 40.334 1.00 40.03 1932 CG ARG B 376 55.132 79.745 41.237 1.00 43.20 1933 CD ARG B 376 54.883 81.198 41.599 1.00 41.05 1934 NE ARG B 376 55.171 81.480 42.992 1.00 50.71 1935 CZ ARG B 376 55.300 82.705 43.488 1.00 53.97 1936 NE1 ARG B 376 55.172 83.758 42.693 1.00 51.88 1937 NH2 ARG B 376 55.542 82.874 44.782 1.00 55.55 1938 N ALA B 377 57.281 79.129 37.122 1.00 40.20 1939 CA ALA B 377 58.382 79.273 36.181 1.00 40.25 1940 C ALA B 377 59.500 80.130 36.786 1.00 40.38 1941 O ALA B 377 60.657 79.979 36.422 1.00 41.16 1942 CB ALA B 377 57.879 79.903 34.878 1.00 33.12 1943 N SER B 378 59.144 81.015 37.714 1.00 40.21 1944 CA SER B 378 60.109 81.903 38.354 1.00 41.95 1945 C SER B 378 60.906 81.188 39.436 1.00 44.92 1946 O SER B 378 61.866 81.744 39.966 1.00 44.28 1947 CB SER B 378 59.401 83.096 38.992 1.00 40.91 1948 OG SER B 378 58.737 82.693 40.180 1.00 40.09 1949 N GLY B 379 60.493 79.967 39.768 1.00 46.93 1950 CA GLY B 379 61.181 79.195 40.787 1.00 49.77 1951 C GLY B 379 60.716 79.512 42.196 1.00 50.60 1952 O GLY B 379 61.024 78.783 43.142 1.00 52.95 1953 N LYS B 380 59.974 80.605 42.345 1.00 53.72 1954 CA LYS B 380 59.478 80.988 43.657 1.00 54.13 1955 C LYS B 380 58.564 79.911 44.255 1.00 48.16 1956 O LYS B 380 58.087 79.008 43.556 1.00 45.65 1957 CB LYS B 380 58.752 82.338 43.583 1.00 62.44 1958 CG LYS B 380 59.692 83.522 43.390 1.00 67.72 1959 CD LYS B 380 58.975 84.852 43.550 1.00 69.32 1960 CE LYS B 380 59.956 86.013 43.481 1.00 73.14 1961 NZ LYS B 380 59.280 87.333 43.633 1.00 77.37 1962 N PRO B 381 58.323 79.986 45.571 1.00 56.07 1963 CA PRO B 381 57.472 79.014 46.265 1.00 56.46 1964 C PRO B 381 55.993 79.065 45.875 1.00 54.32 1965 O PRO B 381 55.446 80.133 45.589 1.00 56.76 1966 CB PRO B 381 57.664 79.375 47.740 1.00 60.70 1967 CG PRO B 381 58.978 80.119 47.767 1.00 62.01 1968 CD PRO B 381 58.905 80.945 46.526 1.00 59.24 1969 N VAL B 382 55.356 77.899 45.866 1.00 55.74 1970 CA VAL B 382 53.931 77.805 45.569 1.00 55.58 1971 C VAL B 382 53.247 77.408 46.880 1.00 55.56 1972 O VAL B 382 53.848 76.734 47.720 1.00 55.22 1973 CB VAL B 382 53.620 76.726 44.493 1.00 55.39 1974 CD1 VAL B 382 54.404 77.008 43.222 1.00 55.94 1975 CG2 VAL B 382 53.936 75.339 45.025 1.00 53.06 1976 N ASN B 383 52.000 77.827 47.055 1.00 54.38 1977 CA ASN B 383 51.246 77.510 48.264 1.00 54.63 1978 C ASN B 383 50.757 76.068 48.290 1.00 53.85 1979 O ASN B 383 50.970 75.297 47.354 1.00 52.58 1980 CB ASN B 383 50.034 78.429 48.382 1.00 59.07 1981 CG ASN B 383 50.414 79.883 48.456 1.00 64.60 1982 OD1 ASN B 383 49.576 80.764 48.269 1.00 70.14 1983 ND2 ASN B 383 51.685 80.150 48.738 1.00 71.07 1984 N HIS B 384 50.094 75.710 49.381 1.00 53.46 1985 CA HIS B 384 49.543 74.371 49.526 1.00 52.22 1986 C HIS B 384 48.298 74.274 48.640 1.00 49.10 1987 O HIS B 384 47.495 75.200 48.585 1.00 45.53 1988 CB HIS B 384 49.183 74.111 50.993 1.00 59.11 1989 CG HIS B 384 50.377 73.924 51.878 1.00 62.16 1990 ND1 HIS B 384 51.243 72.862 51.739 1.00 69.15 1991 CD2 HIS B 384 50.855 74.669 52.903 1.00 70.28 1992 CE1 HIS B 384 52.206 72.960 52.639 1.00 75.01 1993 NE2 HIS B 384 51.995 74.047 53.358 1.00 74.58 1994 N SER B 385 48.146 73.152 47.949 1.00 45.07 1995 CA SER B 385 47.017 72.959 47.060 1.00 44.61 1996 C SER B 385 45.973 71.983 47.604 1.00 44.58 1997 O SER B 385 46.244 71.220 48.521 1.00 44.21 1998 CB SER B 385 47.524 72.487 45.691 1.00 44.61 1999 DC SER B 385 48.310 71.307 45.789 1.00 41.13 2000 N THR B 386 44.773 72.025 47.035 1.00 44.32 2001 CA THR B 386 43.684 71.150 47.446 1.00 44.35 2002 C THR B 386 43.444 70.113 46.363 1.00 44.09 2003 O THR B 386 43.274 70.451 45.189 1.00 44.06 2004 CB THR B 386 42.374 71.936 47.680 1.00 45.20 2005 OG1 THR B 386 42.555 72.856 48.762 1.00 51.89 2006 CG2 THR B 386 41.232 70.984 48.036 1.00 47.20 2007 N ARG B 387 43.424 68.851 46.774 1.00 44.39 2008 CA ARG B 387 43.222 67.730 45.867 1.00 46.68 2009 C ARG B 387 41.837 67.080 46.030 1.00 47.05 2010 O ARG B 387 41.372 66.850 47.149 1.00 46.65 2011 CB ARG B 387 44.316 66.694 46.121 1.00 48.13 2012 CG ARG B 387 44.270 65.488 45.210 1.00 52.77 2013 CD ARG B 387 45.106 64.353 45.780 1.00 56.60 2014 NE ARG B 387 44.978 63.141 44.979 1.00 60.65 2015 CZ ARG B 387 45.683 62.895 43.882 1.00 61.97 2016 NH1 ARG B 387 46.578 63.779 43.464 1.00 64.45 2017 NH2 ARG B 387 45.469 61.781 43.189 1.00 60.54 2018 N LYS B 388 41.185 66.780 44.910 1.00 46.93 2019 CA LYS B 388 39.870 66.143 44.933 1.00 47.51 2020 C LYS B 388 39.823 64.970 43.957 1.00 48.33 2021 O LYS B 388 40.199 65.107 42.794 1.00 46.08 2022 CB LYS B 388 38.777 67.148 44.563 1.00 46.64 2023 CC LYS B 388 38.691 68.326 45.497 1.00 52.75 2024 CD LYS B 388 37.861 69.446 44.905 1.00 58.62 2025 CE LYS B 388 38.062 70.737 45.682 1.00 62.49 2026 NZ LYS B 388 37.396 71.881 44.999 1.00 67.33 2027 N GLU B 389 39.364 63.820 44.449 1.00 50.07 2028 CA GLU B 389 39.243 62.602 43.646 1.00 51.86 2029 C GLU B 389 37.793 62.126 43.638 1.00 52.81 2030 O GLU B 389 37.192 61.917 44.695 1.00 49.21 2031 CB CLO B 389 40.126 61.494 44.223 1.00 54.67 2032 CC GLU B 389 41.616 61.710 44.044 1.00 65.65 2033 CD GLU B 389 42.441 60.608 44.688 1.00 72.66 2034 GE1 GLU B 389 42.151 59.418 44.429 1.00 75.92 2035 OE2 GLU B 389 43.380 60.931 45.450 1.00 75.78 2036 N GLU B 390 37.229 61.948 42.449 1.00 56.06 2037 CA GLU B 390 35.849 61.500 42.346 1.00 61.17 2038 C GLU B 390 35.629 60.454 41.265 1.00 64.70 2039 O GLU B 390 36.072 60.598 40.123 1.00 64.01 2040 CB GLU B 390 34.927 62.692 42.107 1.00 64.35 2041 CC GLU B 390 33.479 62.317 41.867 1.00 74.80 2042 CD GLU B 390 32.548 63.509 41.979 1.00 85.97 2043 OE1 GLU B 390 32.822 64.547 41.336 1.00 92.60 2044 OE2 GLU B 390 31.541 63.403 42.712 1.00 92.18 2045 N LYS B 391 34.921 59.396 41.639 1.00 68.18 2046 CA LYS B 391 34.640 58.312 40.712 1.00 71.58 2047 C LYS B 391 33.215 58.302 40.180 1.00 76.11 2048 O LYS B 391 32.265 58.673 40.869 1.00 75.89 2049 CB LYS B 391 34.946 56.973 41.372 1.00 67.28 2050 N GLN B 392 33.092 57.876 38.932 1.00 81.85 2051 CA GLN B 392 31.814 57.746 38.254 1.00 88.38 2052 C GLN B 392 32.026 56.482 37.443 1.00 92.30 2053 O GLN B 392 32.752 56.500 36.452 1.00 93.25 2054 CB GLN B 392 31.555 58.938 37.323 1.00 85.87 2055 CG CLN B 392 30.422 59.848 37.782 1.00 90.76 2056 CD GLN B 392 30.027 60.873 36.731 1.00 93.39 2057 OE1 GLN B 392 29.687 60.524 35.598 1.00 92.93 2058 NE2 GLN B 392 30.062 62.147 37.107 1.00 93.97 2059 N ARG B 393 31.426 55.379 37.880 1.00 96.24 2060 CA ARG B 393 31.589 54.108 37.184 1.00 100.53 2061 C ARG B 393 31.250 54.188 35.697 1.00 102.30 2062 O ARG B 393 31.273 53.178 34.993 1.00 101.15 2063 CB ARG B 393 30.747 53.021 37.855 1.00 106.99 2064 CG ARG B 393 29.251 53.196 37.704 1.00 109.77 2065 CD ARG B 393 28.521 52.107 38.464 1.00 115.73 2066 NE ARG B 393 27.095 52.085 38.165 1.00 119.73 2067 CZ ARG B 393 26.227 51.267 38.750 1.00 121.60 2068 NH1 ARG B 393 26.645 50.406 39.670 1.00 121.59 2069 NH2 ARG B 393 24.945 51.308 38.416 1.00 121.49 2070 N ASM B 394 30.942 55.391 35.224 1.00 103.98 2071 CA ASN B 394 30.630 55.595 33.819 1.00 106.60 2072 C ASN B 394 31.918 55.325 33.049 1.00 106.89 2073 O ASN B 394 31.950 54.516 32.122 1.00 108.55 2074 CB ASN B 394 30.173 57.036 33.580 1.00 108.97 2075 CG ASN B 394 29.709 57.274 32.153 1.00 112.83 2076 OD1 ASN B 394 29.459 58.410 31.752 1.00 114.53 2077 ND2 ASN B 394 29.584 56.198 31.381 1.00 114.40 2078 N CLY B 395 32.984 56.007 33.452 1.00 105.53 2079 CA CLY B 395 34.269 55.829 32.802 1.00 101.15 2080 C CLY B 395 35.177 57.015 33.050 1.00 97.82 2081 O CLY B 395 35.879 57.475 32.148 1.00 99.41 2082 N THR B 396 35.177 57.516 34.278 1.00 94.50 2083 CA ThR B 396 36.011 58.663 34.578 1.00 89.02 2084 C THR B 396 36.426 58.837 36.029 1.00 83.93 2085 O THR B 396 35.600 59.123 36.896 1.00 83.27 2086 CB THR B 396 35.322 59.975 34.130 1.00 92.03 2087 OC1 THR B 396 35.116 59.952 32.712 1.00 94.17 2088 CG2 THR B 396 36.179 61.186 34.504 1.00 95.48 2089 N LEU B 397 37.718 58.658 36.279 1.00 79.69 2090 CA LEU B 397 38.280 58.871 37.600 1.00 74.75 2091 C LEU B 397 38.773 60.305 37.496 1.00 71.50 2092 O LEU B 397 39.880 60.548 37.019 1.00 74.81 2093 CB LEU B 397 39.480 57.960 37.860 1.00 75.72 2094 CG LEU B 397 40.350 58.412 39.047 1.00 70.67 2095 CD1 LEU B 397 39.742 57.932 40.362 1.00 69.05 2096 CD2 LEU B 397 41.768 57.877 38.887 1.00 72.96 2097 N THR B 398 37.941 61.252 37.905 1.00 67.61 2098 CA THR B 398 38.314 62.655 37.848 1.00 61.30 2099 C THR B 398 39.207 63.041 39.024 1.00 56.61 2100 O THR B 398 38.974 62.640 40.166 1.00 54.95 2101 CB THR B 398 37.070 63.556 37.852 1.00 61.75 2102 OC1 THR B 398 36.345 63.375 36.629 1.00 65.40 2103 CG2 THR B 398 37.471 65.016 37.992 1.00 63.39 2104 N VAL B 399 40.241 63.817 38.729 1.00 51.84 2105 CA VAL B 399 41.163 64.279 39.751 1.00 48.05 2106 C VAL B 399 41.515 65.730 39.490 1.00 44.81 2107 O VAL B 399 41.911 66.098 38.381 1.00 44.41 2108 CB VAL B 399 42.466 63.468 39.751 1.00 49.35 2109 CG1 VAL B 399 43.409 64.010 40.805 1.00 49.43 2110 CG2 VAL B 399 42.168 62.006 40.010 1.00 53.10 2111 N THR B 400 41.354 66.564 40.504 1.00 42.44 2112 CA THR B 400 41.691 67.965 40.343 1.00 40.44 2113 C THR B 400 42.532 68.449 41.498 1.00 38.07 2114 O THR B 400 42.483 67.908 42.602 1.00 36.13 2115 CB THR B 400 40.448 68.869 40.266 1.00 39.64 2116 OG1 THR B 400 39.845 68.962 41.561 1.00 43.72 2117 CG2 THR B 400 39.442 68.322 39.278 1.00 38.32 2118 N SER B 401 43.335 69.460 41.216 1.00 36.90 2119 CA SER B 401 44.168 70.069 42.224 1.00 35.46 2120 C SER B 401 43.988 71.557 42.016 1.00 33.95 2121 O SER B 401 44.153 72.062 40.908 1.00 34.80 2122 CB SER B 401 45.638 69.694 42.040 1.00 36.91 2123 OG SER B 401 46.417 70.301 43.060 1.00 40.84 2124 N THR B 402 43.635 72.248 43.086 1.00 32.28 2125 CA THR B 402 43.422 73.672 43.032 1.00 31.85 2126 C THR B 402 44.508 74.355 43.836 1.00 31.76 2127 O THR B 402 44.737 74.046 45.010 1.00 30.55 2128 CB THR B 402 42.051 74.030 43.595 1.00 31.33 2129 OG1 THR B 402 41.058 73.316 42.862 1.00 32.83 2130 CG2 THR B 402 41.782 75.522 43.468 1.00 32.70 2131 N LEU B 403 45.167 75.301 43.188 1.00 30.72 2132 CA LEU B 403 46.257 76.018 43.800 1.00 30.33 2133 C LEU B 403 45.927 77.485 44.003 1.00 29.66 2134 O LEU B 403 45.608 78.185 43.048 1.00 28.06 2135 CB LEU B 403 47.502 75.902 42.913 1.00 28.34 2136 CG LEU B 403 48.769 76.632 43.381 1.00 32.10 2137 CD1 LEU B 403 49.425 75.823 44.503 1.00 31.94 2138 CD2 LEU B 403 49.756 76.790 42.224 1.00 30.42 2139 N PRO B 404 45.983 77.962 45.259 1.00 31.48 2140 CA PRO B 404 45.704 79.367 45.566 1.00 33.20 2141 C PRO B 404 46.841 80.149 44.906 1.00 34.02 2142 O PRO B 404 47.999 79.755 44.996 1.00 32.25 2143 CB PRO B 404 45.788 79.417 47.090 1.00 33.28 2144 CG PRO B 404 45.435 78.010 47.500 1.00 31.82 2145 CD PRO B 404 46.186 77.187 46.497 1.00 31.26 2146 N VAL B 405 46.503 81.238 44.235 1.00 34.94 2147 CA VAL B 405 47.483 82.044 43.536 1.00 38.63 2148 C VAL B 405 47.541 83.472 44.068 1.00 40.02 2149 O VAL B 405 46.537 84.027 44.502 1.00 40.31 2150 CB VAL B 405 47.143 82.052 42.018 1.00 42.09 2151 CD1 VAL B 405 47.110 83.472 41.468 1.00 43.95 2152 CG2 VAL B 405 48.144 81.195 41.273 1.00 41.76 2153 N GLY B 406 48.728 84.064 44.039 1.00 42.35 2154 CA GLY B 406 48.859 85.432 44.503 1.00 43.35 2155 C GLY B 406 48.178 86.354 43.513 1.00 43.87 2156 O GLY B 406 48.286 86.154 42.303 1.00 42.68 2157 N THR B 407 47.466 87.352 44.023 1.00 44.40 2158 CA THR B 407 46.760 88.306 43.177 1.00 47.37 2159 C THR B 407 47.713 89.127 42.322 1.00 48.27 2160 O TNR B 407 47.549 89.208 41.107 1.00 48.77 2161 CB THR B 407 45.922 89.288 44.022 1.00 48.44 2262 OG1 THR B 407 44.809 88.599 44.596 1.00 50.00 2163 CG2 THR B 407 45.413 90.436 43.162 1.00 53.23 2164 N ARG B 408 48.697 89.746 42.970 1.00 48.10 2165 CA ARG B 408 49.665 90.579 42.279 1.00 48.54 2166 C ARG B 408 50.540 89.773 41.335 1.00 48.48 2167 O ARG B 408 50.769 90.182 40.197 1.00 47.34 2168 CB ARG B 408 50.530 91.325 43.290 1.00 50.16 2169 N ASP B 409 51.033 88.634 41.806 1.00 48.72 2170 CA ASP B 409 51.886 87.787 40.979 1.00 50.88 2171 C ASP B 409 51.187 87.421 39.674 1.00 49.92 2172 O ASP B 409 51.789 87.468 38.598 1.00 49.76 2173 CB ASP B 409 52.260 86.512 41.738 1.00 56.18 2174 CG ASP B 409 53.013 86.801 43.026 1.00 64.80 2175 OD1 ASP B 409 54.062 87.482 42.956 1.00 71.41 2176 OD2 ASP B 409 52.561 86.353 44.105 1.00 68.29 2177 N TRP B 410 49.908 87.067 39.773 1.00 48.36 2178 CA TRP B 410 49.142 86.686 38.597 1.00 46.32 2179 C TRP B 410 48.953 87.864 37.653 1.00 46.21 2180 O TRP B 410 49.111 87.731 36.440 1.00 44.64 2181 CB TRP B 410 47.774 86.120 38.992 1.00 42.82 2182 CG TRP B 410 47.001 85.710 37.796 1.00 39.31 2183 CD1 TRP B 410 46.104 86.467 37.103 1.00 37.29 2184 CD2 TRP B 410 47.181 84.507 37.043 1.00 35.49 2185 NE1 TRP B 410 45.726 85.819 35.957 1.00 39.24 2186 CE2 TRP B 410 46.372 84.613 35.895 1.00 32.76 2187 CE3 TRP B 410 47.956 83.351 37.228 1.00 32.07 2188 CZ2 TRP B 410 46.309 83.606 34.924 1.00 29.59 2189 CZ3 TRP B 410 47.896 82.352 36.269 1.00 33.68 2190 CH2 TRP B 410 47.073 82.489 35.125 1.00 30.56 2191 N ILE B 411 48.611 89.016 38.212 1.00 48.11 2192 CA ILE B 411 48.408 90.209 37.401 1.00 50.90 2193 C ILE B 411 49.712 90.649 36.742 1.00 52.46 2194 O ILE B 411 49.698 91.229 35.658 1.00 53.34 2195 CB ILE B 411 47.845 91.366 38.246 1.00 51.58 2196 CG1 ILE B 411 46.456 90.987 38.770 1.00 52.81 2197 CG2 ILE B 411 47.772 92.634 37.415 1.00 51.95 2198 CD1 ILE B 411 45.823 92.034 39.669 1.00 59.38 2199 N GLU B 412 50.837 90.348 37.385 1.00 53.21 2200 CA GLU B 412 52.137 90.728 36.852 1.00 53.12 2201 C GLU B 412 52.681 89.747 35.831 1.00 51.24 2202 O GLU B 412 53.736 89.990 35.252 1.00 51.40 2203 CB GLU B 412 53.152 90.909 37.981 1.00 59.71 2204 CG GLU B 412 53.022 92.238 38.717 1.00 70.52 2205 CD GLU B 412 54.060 92.399 39.810 1.00 78.58 2206 OE1 GLU B 412 55.262 92.198 39.527 1.00 83.44 2207 OE2 GLU B 412 53.676 92.732 40.950 1.00 82.10 2208 N GLY B 413 51.982 88.634 35.623 1.00 48.47 2209 CA GLY B 413 52.427 87.677 34.626 1.00 44.62 2210 C GLY B 413 53.116 86.387 35.032 1.00 44.15 2211 O GLY B 413 53.687 85.718 34.173 1.00 43.50 2212 N GLU B 414 53.085 86.012 36.307 1.00 42.78 2213 CA GLU B 414 53.722 84.757 36.694 1.00 40.78 2214 C GLU B 414 53.105 83.652 35.851 1.00 39.97 2215 O GLU B 414 51.955 83.758 35.410 1.00 37.43 2216 CB GLU B 414 S3.489 84.445 38.182 1.00 41.96 2217 CG GLU B 414 S4.034 83.081 38.659 1.00 44.09 2218 CD GLU B 414 55.564 83.018 38.740 1.00 49.01 2219 OE1 GLU B 414 56.213 82.549 37.775 1.00 46.84 2220 OE2 GLU B 414 56.121 83.448 39.773 1.00 49.89 2221 N THR B 415 53.879 82.599 35.615 1.00 39.56 2222 CA THR B 415 53.403 81.464 34.847 1.00 40.76 2223 C THR B 415 53.487 80.231 35.738 1.00 40.07 2224 O THR B 415 54.533 79.960 36.323 1.00 42.10 2225 CB THR B 415 54.238 81.273 33.556 1.00 44.69 2226 OG1 THR B 415 54.222 79.893 33.171 1.00 51.98 2227 CG2 THR B 415 55.652 81.744 33.758 1.00 50.00 2228 N TYR B 416 52.380 79.500 35.860 1.00 37.57 2229 CA TYR B 416 52.327 78.318 36.714 1.00 34.50 2230 C TYR B 416 52.265 77.051 35.899 1.00 36.77 2231 O TYR B 416 51.706 77.038 34.800 1.00 35.94 2232 CB TYR B 416 51.116 78.379 37.634 1.00 34.15 2233 CG TYR B 416 51.085 79.597 38.514 1.00 30.65 2234 CD1 TYR B 416 50.777 80.856 37.992 1.00 32.53 2235 CD2 TYR B 416 51.389 79.499 39.865 1.00 31.72 2236 CE1 TYR B 416 50.772 81.984 38.803 1.00 34.27 2237 CE2 TYR B 416 51.390 80.619 40.680 1.00 32.11 2238 CZ TYR B 416 51.080 81.856 40.144 1.00 33.86 2239 OH TYR B 416 51.082 82.964 40.961 1.00 41.22 2240 N GLN B 417 52.829 75.976 36.441 1.00 37.58 2241 CA GLN B 417 52.848 74.722 35.714 1.00 39.43 2242 C GLN B 417 52.341 73.538 36.518 1.00 39.40 2243 O GLN B 417 52.664 73.373 37.694 1.00 39.63 2244 CB GLN B 417 54.269 74.421 35.211 1.00 41.37 2245 CG GLN B 417 54.350 73.214 34.278 1.00 51.81 2246 CD GLN B 417 55.773 72.856 33.886 1.00 61.69 2247 CE1 GLN B 417 56.555 72.371 34.710 1.00 67.15 2248 NE2 GLN B 417 56.119 73.096 32.621 1.00 63.64 2249 N CYS B 418 51.543 72.712 35.864 1.00 39.29 2250 CA CYS B 418 51.019 71.517 36.489 1.00 41.80 2251 C CYS B 418 51.720 70.350 35.818 1.00 42.50 2252 O CYS B 418 51.646 70.191 34.600 1.00 43.33 2253 CB CYS B 418 49.501 71.392 36.275 1.00 41.95 2254 SC CYS B 418 48.795 69.904 37.057 1.00 54.15 2255 N ARG B 419 52.418 69.551 36.609 1.00 43.98 2256 CA ARG B 419 53.103 68.375 36.093 1.00 47.51 2257 C ARG B 419 52.277 67.172 36.542 1.00 48.11 2258 O ARG B 419 52.219 66.859 37.730 1.00 47.85 2259 CB ARG B 419 54.532 68.311 36.648 1.00 49.08 2260 CG ARG B 419 55.203 66.958 36.514 1.00 54.11 2261 CD ARG B 419 56.708 67.046 36.796 1.00 64.71 2262 NE ARG B 419 57.325 65.732 36.963 1.00 64.09 2263 CZ ARG B 419 57.437 65.107 38.132 1.00 70.31 2264 NE1 ARG B 419 56.981 65.681 39.239 1.00 68.32 2265 NH2 ARG B 419 57.992 63.901 38.195 1.00 71.53 2266 N VAL B 420 51.610 66.524 35.592 1.00 51.04 2267 CA VAL B 420 50.776 65.369 35.900 1.00 56.22 2268 C VAL B 420 51.561 64.068 35.746 1.00 61.25 2269 O VAL B 420 52.178 63.820 34.707 1.00 60.11 2270 CB VAL B 420 49.536 65.305 34.985 1.00 54.44 2271 CG1 VAL B 420 48.678 64.106 35.371 1.00 52.69 2272 CG2 VAL B 420 48.732 66.597 35.095 1.00 55.45 2273 N THR B 421 51.529 63.241 36.786 1.00 66.23 2274 CA THR B 421 52.244 61.969 36.774 1.00 73.18 2275 C THR B 421 51.334 60.766 36.970 1.00 76.87 2276 O THR B 421 50.968 60.443 38.100 1.00 77.93 2277 CB THR B 421 53.317 61.929 37.875 1.00 73.75 2278 OG1 THR B 421 54.272 62.972 37.649 1.00 77.71 2279 CG2 THR B 421 54.033 60.591 37.873 1.00 75.35 2280 N HIS B 422 50.976 60.101 35.874 1.00 81.02 2281 CA HIS B 422 50.117 58.922 35.949 1.00 86.07 2282 C HIS B 422 51.004 57.686 35.822 1.00 89.67 2283 O HIS B 422 51.920 57.653 35.002 1.00 90.00 2284 CB HIS B 422 49.071 58.940 34.831 1.00 87.43 2285 CG HIS B 422 47.892 58.052 35.092 1.00 90.73 2286 ND1 HIS B 422 47.076 58.203 36.191 1.00 93.83 2287 CD2 HIS B 422 47.396 57.000 34.396 1.00 91.89 2288 CE1 HIS B 422 46.127 57.282 36.164 1.00 94.70 2289 NE2 HIS B 422 46.300 56.540 35.085 1.00 93.25 2290 N PRO B 423 50.729 56.646 36.626 1.00 92.64 2291 CA PRO B 423 51.489 55.391 36.640 1.00 95.19 2292 C PRO B 423 51.972 54.762 35.325 1.00 97.06 2293 O PRO B 423 53.169 54.536 35.155 1.00 97.57 2294 CB PRO B 423 50.576 54.445 37.433 1.00 95.56 2295 CG PRO B 423 49.209 55.034 37.247 1.00 93.94 2296 CD PRO B 423 49.488 56.495 37.404 1.00 93.12 2297 N HIS B 424 51.058 54.495 34.399 1.00 98.71 2298 CA HIS B 424 51.410 53.831 33.143 1.00 100.16 2299 C HIS B 424 52.104 54.579 32.005 1.00 99.67 2300 O HIS B 424 52.910 53.991 31.284 1.00 99.61 2301 CB HIS B 424 50.165 53.149 32.578 1.00 102.42 2302 CG HIS B 424 49.578 52.125 33.495 1.00 105.47 2303 ND1 HIS B 424 48.302 52.228 34.008 1.00 107.10 2304 CD2 HIS B 424 50.079 50.961 33.967 1.00 97.46 2305 CE1 HIS B 424 48.044 51.170 34.755 1.00 106.81 2306 NE2 HIS B 424 49.106 50.385 34.747 1.00 106.61 2307 N LEU B 425 51.802 55.858 31.833 1.00 99.19 2308 CA LEU B 425 52.384 56.628 30.737 1.00 99.01 2309 C LEU B 425 53.886 56.908 30.816 1.00 98.36 2310 O LEU B 425 54.440 57.121 31.896 1.00 98.39 2311 CB LEU B 425 51.606 57.929 30.593 1.00 100.66 2312 CG LEU B 425 50.105 57.631 30.633 1.00 101.95 2313 CD1 LEU B 425 49.315 58.917 30.531 1.00 102.59 2314 CD2 LEU B 425 49.744 56.677 29.502 1.00 103.85 2315 N PRO B 426 54.562 56.915 29.652 1.00 97.57 2316 CA PRO B 426 56.004 57.165 29.560 1.00 96.82 2317 C PRO B 426 56.414 58.525 30.108 1.00 95.53 2318 O PRO B 426 57.040 58.610 31.163 1.00 95.77 2319 CB PRO B 426 56.282 57.030 28.063 1.00 97.13 2320 CG PRO B 426 54.995 57.494 27.440 1.00 97.88 2321 CD PRO B 426 53.969 56.798 28.307 1.00 97.70 2322 N ARG B 427 56.064 59.585 29.387 1.00 94.16 2323 CA ARG B 427 56.402 60.931 29.826 1.00 92.52 2324 C ARG B 427 55.285 61.509 30.692 1.00 89.85 2325 O ARG B 427 54.123 61.113 30.583 1.00 89.26 2326 CB ARG B 427 56.652 61.851 28.622 1.00 97.34 2327 CG ARG B 427 57.202 63.219 29.023 1.00 99.32 2328 CD ARG B 427 57.407 64.172 27.847 1.00 105.99 2329 NE ARG B 427 58.068 65.403 28.285 1.00 111.10 2330 CZ ARG B 427 58.302 66.460 27.512 1.00 111.66 2331 NH1 ARG B 427 57.927 66.457 26.239 1.00 111.70 2332 NH2 ARG B 427 58.921 67.522 28.013 1.00 110.09 2333 N ALA B 428 55.651 62.442 31.562 1.00 86.56 2334 CA ALA B 428 54.690 63.087 32.439 1.00 82.70 2335 C ALA B 428 53.998 64.211 31.677 1.00 80.03 2336 O ALA B 428 54.619 64.889 30.861 1.00 80.29 2337 CB ALA B 428 55.400 63.647 33.663 1.00 83.85 2338 N LEU B 429 52.708 64.397 31.936 1.00 76.76 2339 CA LEU B 429 51.949 65.456 31.285 1.00 72.72 2340 C LEU B 429 52.311 66.780 31.936 1.00 69.67 2341 O LEU B 429 52.472 66.858 33.153 1.00 68.64 2342 CB LEU B 429 50.444 65.208 31.429 1.00 73.60 2343 CG LEU B 429 49.753 64.431 30.307 1.00 73.35 2344 CD1 LEU B 429 48.320 64.102 30.696 1.00 72.09 2345 CD2 LEU B 429 49.787 65.267 29.035 1.00 76.40 2346 N MET B 430 52.447 67.821 31.124 1.00 66.83 2347 CA MET B 430 52.786 69.132 31.651 1.00 64.81 2348 C MET B 430 51.922 70.216 31.026 1.00 61.41 2349 O MET B 430 51.824 70.326 29.801 1.00 60.84 2350 CB MET B 430 54.265 69.427 31.409 1.00 68.22 2351 CG MET B 430 55.184 68.353 31.967 1.00 74.39 2352 SD MET B 430 56.921 68.714 31.713 1.00 83.18 2353 CE MET B 430 56.993 68.764 29.906 1.00 84.12 2354 N ARG B 431 51.288 71.010 31.882 1.00 57.17 2355 CA ARG B 431 50.428 72.094 31.426 1.00 54.04 2356 C ARG B 431 50.848 73.366 32.137 1.00 50.58 2357 O ARG B 431 51.233 73.330 33.304 1.00 50.46 2358 CB ARG B 431 48.959 71.775 31.736 1.00 55.16 2359 CG ARG B 431 48.413 70.564 30.991 1.00 59.24 2360 CD ARG B 431 48.428 70.798 29.489 1.00 63.93 2361 NE ARG B 431 48.014 69.617 28.737 1.00 70.30 2362 CZ ARG B 431 48.043 69.530 27.411 1.00 76.24 2363 NH1 ARG B 431 48.469 70.559 26.683 1.00 77.83 2364 NH2 ARG B 431 47.648 68.415 26.811 1.00 77.12 2365 N SER B 432 50.788 74.488 31.431 1.00 46.92 2366 CA SER B 432 51.163 75.765 32.016 1.00 45.15 2367 C SER B 432 50.118 76.816 31.702 1.00 42.49 2368 O SER B 432 49.382 76.699 30.721 1.00 42.76 2369 CB SER B 432 52.532 76.206 31.490 1.00 44.31 2370 OG SER B 432 52.516 76.284 30.082 1.00 49.96 2371 N THR B 433 50.060 77.851 32.530 1.00 40.28 2372 CA THR B 433 49.078 78.909 32.337 1.00 39.71 2373 C THR B 433 49.604 80.244 32.843 1.00 39.49 2374 O THR B 433 50.414 80.285 33.766 1.00 40.22 2375 CB THR B 433 47.761 78.577 33.078 1.00 38.07 2376 OG1 THR B 433 46.793 79.594 32.805 1.00 39.56 2377 CG2 THR B 433 47.991 78.512 34.582 1.00 36.99 2378 N THR B 434 49.139 81.328 32.226 1.00 39.18 2379 CA THR B 434 49.532 82.687 32.588 1.00 40.70 2380 C THR B 434 48.414 83.635 32.166 1.00 40.23 2381 O THR B 434 47.509 83.236 31.441 1.00 41.18 2382 CB THR B 434 50.816 83.116 31.844 1.00 43.01 2383 OG1 THR B 434 50.548 83.238 30.439 1.00 47.85 2384 CG2 THR B 434 51.874 82.076 31.995 1.00 48.67 2385 N LYS B 435 48.475 84.886 32.604 1.00 40.97 2386 CA LYS B 435 47.450 85.833 32.211 1.00 45.73 2387 C LYS B 435 47.579 85.999 30.702 1.00 48.93 2388 O LYS B 435 48.670 85.890 30.158 1.00 48.49 2389 CB LYS B 435 47.663 87.166 32.906 1.00 45.94 2390 N THR B 436 46.467 86.235 30.018 1.00 52.01 2391 CA THR B 436 46.520 86.429 28.574 1.00 54.88 2392 C THR B 436 46.916 87.878 28.326 1.00 55.70 2393 O THR B 436 46.454 88.777 29.023 1.00 55.21 2394 CB THR B 436 45.146 86.162 27.909 1.00 56.24 2395 OG1 THR B 436 44.798 84.779 28.062 1.00 60.56 2396 CG2 THR B 436 45.188 86.510 26.423 1.00 57.04 2397 N SER B 437 47.790 88.099 27.352 1.00 57.93 2398 CA SER B 437 48.220 89.451 27.020 1.00 60.42 2399 C SER B 437 47.361 89.917 25.851 1.00 60.49 2400 O SER B 437 46.397 89.243 25.477 1.00 60.21 2401 CB SER B 437 49.706 89.467 26.630 1.00 61.57 2402 OC SER B 437 49.949 88.643 25.500 1.00 65.51 2403 N GLY B 438 47.705 91.067 25.279 1.00 60.09 2404 CA GLY B 438 46.934 91.578 24.161 1.00 58.42 2405 C GLY B 438 45.970 92.663 24.589 1.00 57.80 2406 O GLY B 438 45.853 92.952 25.778 1.00 56.51 2407 N PRO B 439 45.267 93.291 23.633 1.00 57.81 2408 CA PRO B 439 44.305 94.358 23.915 1.00 56.19 2409 C PRO B 439 43.178 93.908 24.837 1.00 53.91 2410 O PRO B 439 42.891 92.714 24.953 1.00 53.91 2411 CB PRO B 439 43.794 94.735 22.524 1.00 57.79 2412 CG PRO B 439 44.967 94.453 21.652 1.00 58.60 2413 CD PRO B 439 45.427 93.115 22.179 1.00 60.65 2414 N ARG B 440 42.545 94.878 25.488 1.00 51.09 2415 CA ARG B 440 41.437 94.610 26.398 1.00 48.90 2416 C ARG B 440 40.235 95.380 25.869 1.00 45.83 2417 O ARG B 440 40.398 96.412 25.219 1.00 45.88 2418 CB ARG B 440 41.764 95.099 27.811 1.00 49.95 2419 CG ARG B 440 43.127 94.681 28.329 1.00 59.03 2420 CD ARG B 440 43.227 93.194 28.652 1.00 65.31 2421 NE ARG B 440 44.627 92.786 28.758 1.00 72.31 2422 CZ ARG B 440 45.047 91.614 29.222 1.00 74.99 2423 NH1 ARG B 440 44.181 90.706 29.640 1.00 77.22 2424 NH2 ARG B 440 46.345 91.348 29.263 1.00 78.59 2425 N ALA B 441 39.036 94.873 26.143 1.00 42.09 2426 CA ALA B 441 37.800 95.521 25.713 1.00 39.26 2427 C ALA B 441 36.706 95.124 26.687 1.00 38.22 2428 O ALA B 441 36.566 93.951 27.024 1.00 38.95 2429 CB ALA B 441 37.430 95.089 24.302 1.00 36.56 2430 N ALA B 442 35.934 96.104 27.134 1.00 37.22 2431 CA ALA B 442 34.871 95.861 28.089 1.00 37.60 2432 C ALA B 442 33.721 95.050 27.510 1.00 38.65 2433 O ALA B 442 33.497 95.047 26.302 1.00 40.22 2434 CB ALA B 442 34.352 97.185 28.619 1.00 37.17 2435 N PRO B 443 32.981 94.340 28.378 1.00 38.04 2436 CA PRO B 443 31.835 93.511 27.996 1.00 36.79 2437 C PRO B 443 30.581 94.376 27.857 1.00 38.14 2438 O PRO B 443 30.426 95.364 28.579 1.00 37.39 2439 CB PRO B 443 31.677 92.550 29.179 1.00 36.30 2440 CG PRO B 443 32.968 92.654 29.941 1.00 36.35 2441 CD PRO B 443 33.351 94.088 29.780 1.00 37.85 2442 N GLU B 444 29.706 94.006 26.927 1.00 36.28 2443 CA GLU B 444 28.437 94.699 26.729 1.00 35.57 2444 C GLU B 444 27.429 93.659 27.212 1.00 33.87 2445 O GLU B 444 27.495 92.490 26.809 1.00 33.43 2446 CB GLU B 444 28.217 95.020 25.249 1.00 38.68 2447 N VAL B 445 26.503 94.080 28.067 1.00 30.18 2448 CA VAL B 445 25.530 93.168 28.650 1.00 28.24 2449 C VAL B 445 24.077 93.464 28.289 1.00 28.44 2450 O VAL B 445 23.625 94.600 28.379 1.00 26.78 2451 CB VAL B 445 25.663 93.183 30.195 1.00 28.10 2452 CG1 VAL B 445 24.667 92.230 30.826 1.00 25.56 2453 CG2 VAL B 445 27.079 92.829 30.589 1.00 26.30 2454 N TYR B 446 23.349 92.425 27.897 1.00 27.87 2455 CA TYR B 446 21.949 92.581 27.549 1.00 27.91 2456 C TYR B 446 21.140 91.407 28.076 1.00 27.06 2457 O TYR B 446 21.293 90.274 27.620 1.00 27.96 2458 CB TYR B 446 21.764 92.702 26.026 1.00 26.45 2459 CG TYR B 446 20.311 92.851 25.653 1.00 26.59 2460 CD1 TYR B 446 19.543 93.886 26.195 1.00 28.48 2461 CD2 TYR B 446 19.686 91.941 24.795 1.00 29.02 2462 CE1 TYR B 446 18.183 94.011 25.896 1.00 33.24 2463 CE2 TYR B 446 18.326 92.057 24.484 1.00 31.33 2464 CZ TYR B 446 17.585 93.094 25.041 1.00 36.01 2465 OH TYR B 446 16.248 93.213 24.762 1.00 36.54 2466 N ALA B 447 20.274 91.686 29.040 1.00 28.07 2467 CA ALA B 447 19.450 90.651 29.661 1.00 27.67 2468 C ALA B 447 18.021 90.785 29.168 1.00 29.19 2469 O ALA B 447 17.564 91.898 28.927 1.00 31.10 2470 CB ALA B 447 19.502 90.798 31.169 1.00 23.97 2471 N PHE B 448 17.307 89.671 29.021 1.00 29.56 2472 CA PHE B 448 15.943 89.751 28.522 1.00 32.50 2473 C PHE B 448 15.117 88.525 28.854 1.00 33.67 2474 O PHE B 448 15.650 87.488 29.228 1.00 35.26 2475 CB PHE B 448 15.970 89.941 27.003 1.00 35.29 2476 CG PHE B 448 16.523 88.751 26.262 1.00 37.04 2477 CD1 PHE B 448 15.691 87.688 25.905 1.00 36.66 2478 CD2 PHE B 448 17.886 88.666 25.973 1.00 34.95 2479 CE1 PHE B 448 16.218 86.551 25.276 1.00 40.91 2480 CE2 PHE B 448 18.422 87.534 25.347 1.00 35.99 2481 CZ PHE B 448 17.586 86.477 24.997 1.00 35.15 2482 N ALA B 449 13.804 88.648 28.704 1.00 35.81 2483 CA ALA B 449 12.907 87.534 28.969 1.00 37.63 2484 C ALA B 449 12.347 86.983 27.662 1.00 40.96 2485 O ALA B 449 12.159 87.715 26.697 1.00 40.14 2486 CB ALA B 449 11.769 87.977 29.870 1.00 33.60 2487 N THR B 450 12.091 85.682 27.652 1.00 45.40 2488 CA THR B 450 11.529 84.994 26.505 1.00 50.82 2489 C THR B 450 10.003 85.085 26.602 1.00 53.78 2490 O THR B 450 9.431 84.927 27.683 1.00 54.14 2491 CB THR B 450 11.935 83.510 26.513 1.00 51.45 2492 OG1 THR B 450 13.358 83.408 26.650 1.00 54.12 2493 CG2 THR B 450 11.507 82.831 25.223 1.00 55.58 2494 N PRO B 451 9.325 85.340 25.474 1.00 56.74 2495 CA PRO B 451 7.863 85.443 25.477 1.00 59.05 2496 C PRO B 451 7.209 84.173 26.020 1.00 61.00 2497 O PRO B 451 7.520 83.065 25.579 1.00 59.71 2498 CB PRO B 451 7.527 85.667 24.002 1.00 60.52 2499 CG PRO B 451 8.749 86.338 23.460 1.00 61.14 2500 CD PRO B 451 9.861 85.551 24.119 1.00 59.39 2501 N GLU B 452 6.315 84.328 26.988 1.00 64.30 2502 CA GLU B 452 5.625 83.172 27.542 1.00 69.17 2503 C GLU B 452 4.137 83.348 27.258 1.00 72.61 2504 O GLU B 452 3.394 83.933 28.043 1.00 73.59 2505 CB GLU B 452 5.888 83.040 29.046 1.00 65.66 2506 CG GLU B 452 6.034 81.585 29.523 1.00 61.46 2507 CD GLU B 452 7.283 80.883 28.967 1.00 60.52 2508 OE1 GLU B 452 8.336 81.547 28.849 1.00 63.47 2509 OE2 GLU B 452 7.227 79.666 28.667 1.00 53.34 2510 N TRP B 453 3.731 82.837 26.103 1.00 76.75 2511 CA TRP B 453 2.358 82.907 25.619 1.00 81.00 2512 C TRP B 453 1.573 81.714 26.187 1.00 82.30 2513 O TRP B 453 1.890 80.562 25.885 1.00 82.08 2514 CB TRP B 453 2.409 82.863 24.090 1.00 85.65 2515 CD TRP B 453 1.233 83.418 23.366 1.00 89.76 2516 CD1 TRP B 453 0.679 84.661 23.512 1.00 92.34 2517 CD2 TRP B 453 0.517 82.781 22.305 1.00 94.15 2518 NE1 TRP B 453 0.334 84.836 22.598 1.00 94.99 2519 CE2 TRP B 453 0.455 83.696 21.845 1.00 95.56 2520 CE3 TRP B 453 0.605 81.521 21.693 1.00 95.36 2521 CZ2 TRP B 453 1.335 83.392 20.800 1.00 97.14 2522 CZ3 TRP B 453 0.269 81.220 20.655 1.00 95.61 2523 CH2 TRP B 453 1.226 82.153 20.220 1.00 97.12 2524 N PRO B 454 0.542 81.981 27.020 1.00 84.10 2525 CA PRO B 454 0.331 80.994 27.678 1.00 87.24 2526 C PRO B 454 0.716 79.708 26.938 1.00 90.52 2527 O PRO B 454 0.378 79.512 25.767 1.00 89.75 2528 CB PRO B 454 1.550 81.825 28.112 1.00 84.91 2529 CG PRO B 454 1.417 83.125 27.360 1.00 83.62 2530 CD PRO B 454 0.063 83.341 27.307 1.00 84.60 2531 N GLY B 455 1.455 78.849 27.636 1.00 91.72 2532 CA GLY B 455 1.813 77.552 27.088 1.00 94.13 2533 C GLY B 455 0.532 76.870 27.499 1.00 96.28 2534 O CLY B 455 0.475 76.987 26.799 1.00 97.74 2535 N SER B 456 0.542 76.158 28.622 1.00 99.11 2536 CA SER B 456 0.731 75.626 29.077 1.00 96.15 2537 C SER B 456 1.135 74.193 29.424 1.00 91.50 2538 O SER B 456 0.316 73.308 29.767 1.00 88.52 2539 CB SER B 456 1.222 76.508 30.221 1.00 95.05 2540 OG SER B 456 0.225 76.690 31.216 1.00 110.76 2541 N ARG B 457 2.464 74.059 29.348 1.00 87.73 2542 CA ARG B 457 3.349 72.936 29.580 1.00 87.81 2543 C ARG B 457 4.497 73.922 29.453 1.00 86.30 2544 O ARG B 457 4.602 74.574 28.403 1.00 90.57 2545 CB ARG B 457 3.339 71.966 28.425 1.00 94.67 2546 N ASP B 458 5.341 74.088 30.473 1.00 87.32 2547 CA ASP B 458 6.314 75.159 30.320 1.00 80.43 2548 C ASP B 458 7.637 75.178 31.020 1.00 72.83 2549 O ASP B 458 8.163 74.190 31.501 1.00 73.96 2550 CB ASP B 458 5.615 76.450 30.715 1.00 83.19 2551 CG ASP B 458 5.300 76.498 32.210 1.00 85.09 2552 OD1 ASP B 458 4.694 75.535 32.722 1.00 91.25 2553 OD2 ASP B 458 5.661 77.492 32.883 1.00 90.84 2554 N LYS B 459 8.149 76.404 31.024 1.00 66.05 2555 CA LYS B 459 9.389 76.818 31.663 1.00 61.75 2556 C LYS B 459 9.617 78.232 31.214 1.00 56.14 2557 O LYS B 459 9.952 78.456 30.054 1.00 56.54 2558 CB LYS B 459 10.569 75.959 31.211 1.00 68.18 2559 CG LYS B 459 10.796 74.799 32.131 1.00 71.85 2560 CD LYS B 459 10.737 75.194 33.601 1.00 73.79 2561 CE LYS B 459 10.761 73.945 34.474 1.00 76.14 2562 NZ LYS B 459 10.925 74.259 35.931 1.00 79.35 2563 N ARG B 460 9.406 79.194 32.099 1.00 52.32 2564 CA ARG B 460 9.649 80.565 31.723 1.00 47.59 2565 C ARG B 460 11.164 80.740 31.810 1.00 43.34 2566 O ARG B 460 11.839 80.123 32.638 1.00 40.40 2567 CB ARG B 460 8.874 81.496 32.644 1.00 49.27 2568 CG ARG B 460 7.384 81.325 32.429 1.00 56.23 2569 CD ARG B 460 6.594 81.941 33.568 1.00 63.20 2570 NE ARG B 460 5.174 81.603 33.504 1.00 68.02 2571 CZ ARG B 460 4.645 80.455 33.920 1.00 70.46 2572 NH1 ARG B 460 5.415 79.506 34.444 1.00 72.23 2573 NH2 ARG B 460 3.336 80.264 33.815 1.00 73.53 2574 N THR B 461 11.690 81.538 30.902 1.00 39.19 2575 CA THR B 461 13.126 81.721 30.822 1.00 36.81 2576 C THR B 461 13.596 83.153 30.699 1.00 34.03 2577 O THR B 461 12.993 83.969 29.990 1.00 33.96 2578 CB THR B 461 13.710 80.997 29.588 1.00 39.13 2579 OG1 THR B 461 13.243 79.643 29.543 1.00 46.04 2580 CG2 THR B 461 15.220 80.970 29.679 1.00 45.48 2581 N LEU B 462 14.696 83.443 31.386 1.00 29.84 2582 CA LEU B 462 15.333 84.747 31.312 1.00 28.03 2583 C LEU B 462 16.674 84.395 30.690 1.00 27.33 2584 O LEU B 462 17.186 83.293 30.893 1.00 24.47 2585 CB LEU B 462 15.526 85.377 32.697 1.00 25.97 2586 CG LEU B 462 14.238 85.712 33.465 1.00 33.39 2587 CD1 LEU B 462 14.593 86.428 34.781 1.00 32.36 2588 CD2 LEU B 462 13.337 86.586 32.617 1.00 30.72 2589 N ALA B 463 17.241 85.314 29.922 1.00 25.83 2590 CA ALA B 463 18.489 85.023 29.264 1.00 25.65 2591 C ALA B 463 19.321 86.270 29.143 1.00 26.32 2592 O ALA B 463 18.810 87.386 29.254 1.00 27.53 2593 CB ALA B 463 18.219 84.421 27.888 1.00 28.15 2594 N CYS B 464 20.608 86.082 28.905 1.00 21.23 2595 CA CYS B 464 21.507 87.212 28.824 1.00 24.77 2596 C CYS B 464 22.584 87.001 27.786 1.00 22.14 2597 O CYS B 464 23.169 85.917 27.698 1.00 24.66 2598 CB CYS B 464 22.171 87.407 30.186 1.00 22.04 2599 SG CYS B 464 23.302 88.810 30.380 1.00 34.06 2600 N LEU B 465 22.859 88.052 27.025 1.00 22.44 2601 CA LEU B 465 23.903 88.002 26.011 1.00 23.11 2602 C LEU B 465 24.985 88.956 26.459 1.00 22.43 2603 O LEU B 465 24.702 90.117 26.748 1.00 23.73 2604 CB LEU B 465 23.370 88.445 24.639 1.00 22.99 2605 CG LEU B 465 24.423 88.790 23.562 1.00 19.04 2606 CD1 LEU B 465 25.269 87.565 23.234 1.00 21.72 2607 CD2 LEU B 465 23.716 89.253 22.282 1.00 28.23 2608 N ILE B 466 26.220 88.475 26.519 1.00 22.56 2609 CA ILE B 466 27.332 89.323 26.931 1.00 22.11 2610 C ILE B 466 28.344 89.298 25.803 1.00 24.25 2611 O ILE B 466 28.785 88.225 25.394 1.00 24.93 2612 CB ILE B 466 27.946 88.819 28.239 1.00 22.15 2613 CG1 ILE B 466 26.850 88.751 29.314 1.00 23.07 2614 CG2 ILE B 466 29.075 89.778 28.684 1.00 25.24 2615 CD1 ILE B 466 27.282 88.091 30.604 1.00 33.12 2616 N GLN B 467 28.737 90.468 25.307 1.00 24.63 2617 CA GLN B 467 29.630 90.480 24.149 1.00 28.64 2618 C GLN B 467 30.637 91.618 24.028 1.00 31.08 2619 O GLN B 467 30.685 92.529 24.865 1.00 31.00 2620 CB GLN B 467 28.770 90.428 22.872 1.00 25.58 2621 CG GLN B 467 27.873 91.657 22.696 1.00 25.53 2622 CD GLN B 467 26.907 91.556 21.501 1.00 30.72 2623 OE1 GLN B 467 27.144 90.810 20.551 1.00 29.76 2624 NE2 GLN B 467 25.821 92.327 21.550 1.00 32.18 2625 N ASN B 468 31.453 91.517 22.977 1.00 33.71 2626 CA ASN B 468 32.494 92.486 22.641 1.00 36.96 2627 C ASN B 468 33.601 92.607 23.677 1.00 38.20 2628 O ASN B 468 34.208 93.669 23.812 1.00 38.39 2629 CB ASN B 468 31.881 93.869 22.424 1.00 41.06 2630 CG ASN B 468 30.763 93.852 21.414 1.00 46.41 2631 OD1 ASN B 468 30.879 93.228 20.359 1.00 50.82 2632 ND2 ASN B 468 29.672 94.548 21.724 1.00 53.31 2633 N PHE B 469 33.868 91.535 24.415 1.00 35.74 2634 CA PHE B 469 34.910 91.597 25.423 1.00 33.87 2635 C PHE B 469 36.147 90.796 25.044 1.00 33.63 2636 O PHE B 469 36.087 89.873 24.240 1.00 34.78 2637 CB PHE B 469 34.372 91.105 26.778 1.00 29.12 2638 CG PHE B 469 33.909 89.674 26.766 1.00 26.27 2639 CD1 PHE B 469 34.808 88.641 26.967 1.00 22.45 2640 CD2 PHE B 469 32.566 89.362 26.561 1.00 22.06 2641 CE1 PHE B 469 34.386 87.315 26.974 1.00 23.84 2642 CE2 PHE B 469 32.135 88.036 26.564 1.00 28.02 2643 CZ PHE B 469 33.051 87.007 26.773 1.00 23.33 2644 N MET B 470 37.273 91.169 25.634 1.00 35.64 2645 CA MET B 470 38.535 90.480 25.413 1.00 37.62 2646 C MET B 470 39.496 90.916 26.504 1.00 36.36 2647 O MET B 470 39.478 92.071 26.923 1.00 36.33 2648 CB MET B 470 39.105 90.796 24.024 1.00 42.61 2649 CG MET B 470 39.421 92.246 23.750 1.00 50.60 2650 SD MET B 470 39.856 92.459 21.987 1.00 66.08 2651 CE MET B 470 41.544 91.820 21.966 1.00 66.35 2652 N PRO B 471 40.317 89.987 27.021 1.00 34.63 2653 CA PRO B 471 40.431 88.561 26.682 1.00 32.61 2654 C PRO B 471 39.147 87.782 26.957 1.00 31.92 2655 O PRO B 471 38.164 88.356 27.415 1.00 29.59 2656 CB PRO B 471 41.585 88.080 27.562 1.00 33.95 2657 CG PRO B 471 42.373 89.323 27.805 1.00 37.90 2658 CD PRO B 471 41.309 90.354 28.042 1.00 34.78 2659 N GLU B 472 39.187 86.472 26.714 1.00 32.28 2660 CA GLU B 472 38.020 85.599 26.866 1.00 36.49 2661 C GLU B 472 37.557 85.220 28.270 1.00 35.52 2662 O GLU B 472 36.438 84.730 28.417 1.00 34.87 2663 CB GLU B 472 38.223 84.298 26.085 1.00 41.97 2664 CG GLU B 472 39.294 83.387 26.677 1.00 54.78 2665 CD GLU B 472 39.456 82.073 25.916 1.00 62.41 2666 OE1 GLU B 472 39.021 81.997 24.744 1.00 67.26 2667 OE2 GLU B 472 40.034 81.119 26.487 1.00 64.96 2668 N ASP B 473 38.379 85.439 29.295 1.00 34.38 2669 CA ASP B 473 37.971 85.057 30.648 1.00 31.83 2670 C ASP B 473 36.914 85.998 31.214 1.00 31.24 2671 O ASP B 473 37.072 87.220 31.199 1.00 31.80 2672 CB ASP B 473 39.180 84.979 31.584 1.00 34.73 2673 CG ASP B 473 40.147 83.854 31.196 1.00 40.83 2674 OD1 ASP B 473 39.676 82.759 30.804 1.00 44.18 2675 OD2 ASP B 473 41.378 84.061 31.290 1.00 40.17 2676 N ILE B 474 35.826 85.416 31.702 1.00 26.96 2677 CA ILE B 474 34.744 86.207 32.246 1.00 25.39 2678 C ILE B 474 33.885 85.375 33.208 1.00 24.74 2679 O ILE B 474 33.776 84.164 33.069 1.00 25.20 2680 CB ILE B 474 33.862 86.758 31.092 1.00 23.81 2681 CG1 ILE B 474 32.925 87.852 31.598 1.00 22.23 2682 CG2 ILE B 474 33.062 85.626 30.453 1.00 27.10 2683 CD1 ILE B 474 32.144 88.536 30.450 1.00 25.30 2684 N SER B 475 33.312 86.030 34.209 1.00 23.27 2685 CA SER B 475 32.430 85.348 35.148 1.00 22.17 2686 C SER B 475 31.066 85.991 34.952 1.00 21.71 2687 O SER B 475 30.951 87.207 34.876 1.00 20.84 2688 CB SER B 475 32.879 85.551 36.593 1.00 20.43 2689 00 SER B 475 34.164 85.011 36.806 1.00 30.00 2690 N VAL B 476 30.042 85.158 34.887 1.00 21.76 2691 CA VAL B 476 28.694 85.620 34.675 1.00 21.72 2692 C VAL B 476 27.875 85.165 35.851 1.00 23.56 2693 O VAL B 476 28.036 84.045 36.320 1.00 25.95 2694 CB VAL B 476 28.087 84.994 33.385 1.00 21.56 2695 CG1 VAL B 476 26.625 85.443 33.222 1.00 18.70 2696 CG2 VAL B 476 28.915 85.403 32.166 1.00 20.99 2697 N GLN B 477 26.994 86.026 36.336 1.00 25.16 2698 CA GLN B 477 26.172 85.635 37.460 1.00 26.65 2699 C GLN B 477 24.833 86.337 37.438 1.00 26.62 2700 O GLN B 477 24.709 87.440 36.925 1.00 26.40 2701 CB GLN B 477 26.917 85.899 38.775 1.00 31.51 2702 CG GLN B 477 27.348 87.311 39.011 1.00 44.27 2703 CD GLN B 477 28.505 87.412 40.016 1.00 47.76 2704 OE1 GLN B 477 28.814 88.496 40.502 1.00 50.57 2705 NE2 GLN B 477 29.151 86.283 40.313 1.00 47.32 2706 N TRP B 478 23.820 85.659 37.954 1.00 27.41 2707 CA TRP B 478 22.488 86.225 38.026 1.00 28.36 2708 C TRP B 478 22.192 86.656 39.465 1.00 30.10 2709 O TRP B 478 22.660 86.033 40.428 1.00 25.31 2710 CB TRP B 478 21.461 85.196 37.567 1.00 28.76 2711 CG TRP B 478 21.502 84.951 36.087 1.00 34.11 2712 CD1 TRP B 478 22.313 84.078 35.415 1.00 31.25 2713 CD2 TRP B 478 20.722 85.620 35.094 1.00 31.01 2714 NE1 TRP B 478 22.085 84.164 34.069 1.00 27.71 2715 CE2 TRP B 478 21.113 85.104 33.841 1.00 31.95 2716 CE3 TRP B 478 19.729 86.607 35.140 1.00 34.16 2717 CZ2 TRP B 478 20.542 85.545 32.637 1.00 25.26 2718 CZ3 TRP B 478 19.161 87.044 33.947 1.00 31.64 2719 CH2 TRP B 478 19.571 86.511 32.713 1.00 28.89 2720 N LEU B 479 21.418 87.723 39.602 1.00 32.48 2721 CA LEU B 479 21.049 88.245 40.913 1.00 37.36 2722 C LEU B 479 19.584 88.657 40.960 1.00 40.42 2723 O LEU B 479 19.040 89.152 39.977 1.00 40.14 2724 CB LEU B 479 21.878 89.478 41.252 1.00 39.83 2725 CG LEU B 479 23.346 89.556 40.842 1.00 44.57 2726 CD1 LEU B 479 23.890 90.887 41.290 1.00 52.98 2727 CD2 LEU B 479 24.130 88.439 41.466 1.00 50.71 2728 N HIS B 480 18.947 88.448 42.102 1.00 43.05 2729 CA HIS B 480 17.572 88.877 42.276 1.00 49.20 2730 C HIS B 480 17.746 90.136 43.116 1.00 52.73 2731 O HIS B 480 17.705 90.091 44.347 1.00 52.90 2732 CB HIS B 480 16.754 87.844 43.043 1.00 52.25 2733 CG HIS B 480 15.341 88.270 43.286 1.00 57.22 2734 ND1 HIS B 480 14.337 88.075 42.364 1.00 61.37 2735 CD2 HIS B 480 14.778 88.942 44.319 1.00 59.16 2736 CE1 HIS B 480 13.216 88.607 42.815 1.00 59.88 2737 NE2 HIS B 480 13.456 89.140 44.000 1.00 66.11 2738 N ASN B 481 17.971 91.253 42.430 1.00 56.65 2739 CA ASN B 481 18.206 92.543 43.070 1.00 59.93 2740 C ASN B 481 19.660 92.591 43.519 1.00 59.65 2741 O ASN B 481 20.571 92.569 42.695 1.00 61.04 2742 CB ASN B 481 17.288 92.751 44.282 1.00 64.65 2743 CG ASN B 481 15.852 93.022 43.890 1.00 72.38 2744 OG1 ASN B 481 15.563 93.964 43.147 1.00 74.96 2745 ND2 ASN B 481 14.938 92.199 44.393 1.00 75.60 2746 N GLU B 482 19.872 92.625 44.827 1.00 58.97 2747 CA GLU B 482 21.213 92.697 45.396 1.00 58.55 2748 C GLU B 482 21.815 91.346 45.782 1.00 55.30 2749 O GLU B 482 23.013 91.253 46.044 1.00 57.27 2750 CB GLU B 482 21.176 93.607 46.627 1.00 65.42 2751 CG GLU B 482 19.760 93.813 47.172 1.00 73.94 2752 CD GLU B 482 19.735 94.473 48.532 1.00 80.29 2753 OE1 GLU B 482 20.168 93.830 49.513 1.00 86.31 2754 OE2 GLU B 482 19.284 95.633 48.620 1.00 82.73 2755 N VAL B 483 20.997 90.301 45.814 1.00 50.25 2756 CA VAL B 483 21.487 88.988 46.211 1.00 45.78 2757 C VAL B 483 21.733 88.025 45.052 1.00 43.04 2758 O VAL B 483 20.880 87.834 44.198 1.00 41.34 2759 CB VAL B 483 20.527 88.339 47.233 1.00 43.76 2760 CG1 VAL B 483 19.129 88.283 46.668 1.00 46.25 2761 CG2 VAL B 483 21.011 86.946 47.594 1.00 41.37 2762 N GLN B 484 22.912 87.412 45.050 1.00 42.30 2763 CA GLN B 484 23.300 86.474 44.005 1.00 43.21 2764 C GLN B 484 22.658 85.091 44.141 1.00 42.48 2765 O GLN B 484 22.538 84.545 45.244 1.00 41.64 2766 CB GLN B 484 24.826 86.331 43.971 1.00 45.96 2767 CG GLN B 484 25.324 85.269 42.999 1.00 54.43 2768 CD GLN B 484 26.840 85.173 42.941 1.00 59.02 2769 OE1 GLN B 484 27.391 84.200 42.423 1.00 59.71 2770 NE2 GLN B 484 27.522 86.190 43.464 1.00 61.46 2771 N LEU B 485 22.239 84.539 43.006 1.00 38.99 2772 CA LEU B 485 21.618 83.218 42.953 1.00 39.17 2773 C LEU B 485 22.700 82.142 42.853 1.00 40.35 2774 O LEU B 485 23.822 82.417 42.430 1.00 37.39 2775 CB LEU B 485 20.705 83.107 41.725 1.00 37.16 2776 CG LEU B 485 19.579 84.140 41.602 1.00 39.66 2777 CD1 LEU B 485 18.836 83.930 40.293 1.00 39.30 2778 CD2 LEU B 485 18.644 84.020 42.795 1.00 40.56 2779 N PRO B 486 22.373 80.900 43.242 1.00 42.55 2780 CA PRO B 486 23.366 79.828 43.158 1.00 46.30 2781 C PRO B 486 23.750 79.660 41.688 1.00 49.32 2782 O PRO B 486 22.916 79.852 40.806 1.00 48.81 2783 CB PRO B 486 22.606 78.609 43.675 1.00 45.64 2784 CG PRO B 486 21.532 79.187 44.528 1.00 45.29 2785 CD PRO B 486 21.095 80.394 43.769 1.00 40.65 2786 N ASP B 487 24.997 79.290 41.429 1.00 53.39 2787 CA ASP B 487 25.465 79.093 40.062 1.00 57.75 2788 C ASP B 487 24.660 77.997 39.350 1.00 57.25 2789 O ASP B 487 24.205 78.176 38.213 1.00 57.75 2790 CB ASP B 487 26.944 78.708 40.077 1.00 67.82 2791 CG ASP B 487 27.577 78.779 38.703 1.00 76.17 2792 OD1 ASP B 487 26.945 78.309 37.734 1.00 84.77 2793 OD2 ASP B 487 28.711 79.297 38.592 1.00 86.94 2794 N ALA B 488 24.478 76.873 40.035 1.00 54.64 2795 CA ALA B 488 23.752 75.729 39.493 1.00 53.45 2796 C ALA B 488 22.421 76.069 38.837 1.00 52.74 2797 O ALA B 488 21.843 75.241 38.134 1.00 53.06 2798 CB ALA B 488 23.530 74.708 40.585 1.00 53.75 2799 N ARG B 489 21.938 77.287 39.056 1.00 50.96 2800 CA ARG B 489 20.660 77.704 38.491 1.00 47.84 2801 C ARG B 489 20.705 78.164 37.036 1.00 45.10 2802 O ARG B 489 19.681 78.158 36.363 1.00 43.37 2803 CB ARG B 489 20.046 78.808 39.354 1.00 48.99 2804 CG ARG B 489 19.232 78.294 40.524 1.00 50.01 2805 CD ARG B 489 17.761 78.427 40.227 1.00 50.36 2806 NE ARG B 489 17.187 79.581 40.905 1.00 56.65 2807 CZ ARG B 489 16.048 80.166 40.557 1.00 58.23 2808 NH1 ARG B 489 15.352 79.714 39.522 1.00 61.07 2809 NH2 ARO B 489 15.594 81.193 41.260 1.00 59.63 2810 N HIS B 490 21.872 78.573 36.551 1.00 42.41 2811 CA HIS B 490 21.965 79.024 35.166 1.00 41.63 2812 C HIS B 490 22.952 78.210 34.334 1.00 39.71 2813 O HIS B 490 23.768 77.471 34.865 1.00 41.30 2814 CB HIS B 490 22.348 80.508 35.100 1.00 42.40 2815 CD HIS B 490 23.720 80.807 35.614 1.00 43.27 2816 ND1 HIS B 490 23.966 81.177 36.919 1.00 42.27 2817 CD2 HIS B 490 24.926 80.779 34.999 1.00 44.41 2818 CE1 HIS B 490 25.262 81.364 37.086 1.00 39.88 2819 NE2 HIS B 490 25.868 81.130 35.934 1.00 45.37 2820 N SER B 491 22.858 78.355 33.020 1.00 37.20 2821 CA SER B 491 23.734 77.654 32.095 1.00 36.36 2822 C SER B 491 24.401 78.685 31.173 1.00 33.06 2823 O SER B 491 23.721 79.428 30.461 1.00 33.77 2824 CB SER B 491 22.910 76.651 31.288 1.00 35.42 2825 OG SER B 491 23.694 76.053 30.282 1.00 43.65 2826 N THR B 492 25.728 78.722 31.188 1.00 29.90 2827 CA THR B 492 26.495 79.673 30.383 1.00 29.91 2828 C THR B 492 27.322 78.977 29.287 1.00 29.20 2829 O THR B 492 27.996 77.991 29.552 1.00 30.85 2830 CB THR B 492 27.447 80.506 31.298 1.00 29.85 2831 OG1 THR B 492 26.670 81.197 32.281 1.00 35.86 2832 CG2 THR B 492 28.234 81.541 30.498 1.00 28.05 2833 N THR B 493 27.281 79.505 28.065 1.00 29.49 2834 CA THR B 493 28.032 78.913 26.957 1.00 30.19 2835 C THR B 493 29.501 79.295 27.056 1.00 32.39 2836 O THR B 493 29.863 80.210 27.786 1.00 30.70 2837 CB THR B 493 27.502 79.378 25.568 1.00 27.82 2838 OG1 THR B 493 27.592 80.806 25.460 1.00 30.48 2839 CG2 THR B 493 26.067 78.953 25.372 1.00 22.03 2840 N GLN B 494 30.347 78.586 26.322 1.00 35.09 2841 CA GLN B 494 31.779 78.879 26.330 1.00 38.19 2842 C GLN B 494 32.032 80.091 25.449 1.00 36.48 2843 O GLN B 494 31.360 80.270 24.432 1.00 35.75 2844 CB GLN B 494 32.581 77.696 25.775 1.00 43.09 2845 CD GLN B 494 32.502 76.433 26.610 1.00 58.35 2846 CD GLN B 494 32.929 76.666 28.042 1.00 65.11 2847 OE1 GLN B 494 34.003 77.209 28.303 1.00 71.67 2848 NE2 GLN B 494 32.088 76.255 28.982 1.00 71.87 2849 N PRO B 495 33.002 80.939 25.828 1.00 36.89 2850 CA PRO B 495 33.322 82.130 25.037 1.00 38.37 2851 C PRO B 495 33.609 81.737 23.587 1.00 40.80 2852 O PRO B 495 34.314 80.763 23.327 1.00 40.76 2853 CB PRO B 495 34.557 82.680 25.729 1.00 37.83 2854 CG PRO B 495 34.315 82.300 27.174 1.00 40.41 2855 CD PRO B 495 33.809 80.884 27.061 1.00 35.81 2856 N ARG B 496 33.040 82.480 22.650 1.00 42.05 2857 CA ARG B 496 33.255 82.208 21.240 1.00 47.69 2858 C ARG B 496 33.772 83.454 20.542 1.00 51.66 2859 O ARG B 496 33.283 84.558 20.784 1.00 51.95 2860 CB ARO B 496 31.954 81.751 20.584 1.00 45.81 2861 CG ARG B 496 31.599 80.317 20.892 1.00 51.53 2862 CD ARG B 496 30.217 79.947 20.391 1.00 53.72 2863 NE ARO B 496 30.175 78.554 19.963 1.00 57.50 2864 CZ ARG B 496 30.608 78.122 18.783 1.00 58.59 2865 NH1 ARG B 496 31.111 78.974 17.901 1.00 57.22 2866 NH2 ARG B 496 30.542 76.832 18.488 1.00 65.31 2867 N LYS B 497 34.773 83.281 19.687 1.00 56.98 2868 CA LYS B 497 35.335 84.408 18.953 1.00 61.91 2869 C LYS B 497 34.301 84.867 17.955 1.00 63.97 2870 O LYS B 497 33.300 84.195 17.729 1.00 64.61 2871 CB LYS B 497 36.587 84.003 18.172 1.00 66.35 2872 CG LYS B 497 37.848 83.781 18.987 1.00 74.14 2873 CD LYS B 497 38.993 83.359 18.066 1.00 80.69 2874 CE LYS B 497 40.304 83.192 18.814 1.00 84.48 2875 NZ LYS B 497 41.385 82.739 17.889 1.00 88.26 2876 N THR B 498 34.555 86.017 17.352 1.00 67.67 2877 CA THR B 498 33.669 86.572 16.342 1.00 71.26 2878 C THR B 498 34.550 87.284 15.340 1.00 73.04 2879 O THR B 498 35.743 86.990 15.236 1.00 72.83 2880 CB THR B 498 32.679 87.585 16.945 1.00 71.80 2881 OG1 THR B 498 33.392 88.555 17.721 1.00 71.58 2882 CG THR B 498 31.670 86.878 17.819 1.00 73.61 2883 N LYS B 499 33.962 88.220 14.605 1.00 75.57 2884 CA LYS B 499 34.705 88.993 13.620 1.00 77.62 2885 C LYS B 499 35.427 90.142 14.321 1.00 77.92 2886 O LYS B 499 34.791 91.096 14.768 1.00 79.19 2887 CB LYS B 499 33.752 89.558 12.567 1.00 80.22 2888 CG LYS B 499 33.172 88.531 11.604 1.00 81.04 2889 CD LYS B 499 34.203 88.093 10.571 1.00 83.26 2890 CE LYS B 499 33.569 87.232 9.487 1.00 84.81 2891 NZ LYS B 499 34.545 86.864 8.425 1.00 86.04 2892 N GLY B 500 36.748 90.034 14.433 1.00 76.91 2893 CA GLY B 500 37.544 91.077 15.061 1.00 75.83 2894 C GLY B 500 37.141 91.560 16.445 1.00 75.14 2895 O GLY B 500 37.971 91.576 17.355 1.00 75.52 2896 N SER B 501 35.882 91.958 16.605 1.00 73.08 2897 CA SER B 501 35.370 92.468 17.875 1.00 71.65 2898 C BER B 501 36.008 91.836 19.106 1.00 68.64 2899 O SER B 501 36.690 92.515 19.877 1.00 71.13 2900 CB SER B 501 33.854 92.279 17.953 1.00 74.43 2901 OG SER B 501 33.524 90.933 18.241 1.00 80.92 2902 N GLY B 502 35.786 90.540 19.290 1.00 63.14 2903 CA GLY B 502 36.344 89.859 20.443 1.00 54.62 2904 C GLY B 502 35.552 88.618 20.803 1.00 48.04 2905 O GLY B 502 35.469 87.683 20.006 1.00 48.08 2906 N PHE B 503 34.958 88.599 21.994 1.00 40.50 2907 CA PHE B 503 34.189 87.427 22.408 1.00 33.81 2908 C PHE B 503 32.773 87.692 22.888 1.00 28.39 2909 O PHE B 503 32.408 88.811 23.244 1.00 26.35 2910 CB PHE B 503 34.919 86.662 23.517 1.00 35.09 2911 CG PHE B 503 36.263 86.148 23.119 1.00 34.16 2912 CD1 PHE B 503 37.381 86.970 23.174 1.00 35.05 2913 CD2 PHE B 503 36.411 84.845 22.670 1.00 35.90 2914 CE1 PHE B 503 38.633 86.501 22.783 1.00 36.00 2915 CE2 PHE B 503 37.656 84.362 22.274 1.00 40.04 2916 CZ PHE B 503 38.771 85.192 22.329 1.00 38.82 2917 N PHE B 504 31.975 86.633 22.884 1.00 26.16 2918 CA PHE B 504 30.612 86.709 23.369 1.00 25.00 2919 C PHE B 504 30.286 85.418 24.096 1.00 26.57 2920 O PHE B 504 30.892 84.379 23.833 1.00 26.73 2921 CB PHE B 504 29.616 86.960 22.242 1.00 22.46 2922 CG PHE B 504 29.330 85.766 21.382 1.00 27.70 2923 CD1 PHE B 504 28.260 84.926 21.667 1.00 28.94 2924 CD2 PHE B 504 30.086 85.517 20.243 1.00 31.34 2925 CE1 PHE B 504 27.938 83.857 20.827 1.00 30.08 2926 CE2 PHE B 504 29.772 84.449 19.396 1.00 32.65 2927 CZ PHE B 504 28.691 83.621 19.697 1.00 32.80 2928 N VAL B 505 29.330 85.509 25.015 1.00 23.68 2929 CA VAL B 505 28.895 84.389 25.814 1.00 24.67 2930 C VAL B 505 27.385 84.559 26.028 1.00 23.86 2931 O VAL B 505 26.875 85.672 26.051 1.00 21.24 2932 CB VAL B 505 29.674 84.392 27.161 1.00 27.95 2933 CG1 VAL B 505 29.136 85.466 28.080 1.00 25.61 2934 CG2 VAL B 505 29.643 83.042 27.786 1.00 33.51 2935 N PHE B 506 26.664 83.454 26.141 1.00 26.20 2936 CA PHE B 506 25.218 83.514 26.346 1.00 26.10 2937 C PHE B 506 24.855 82.754 27.621 1.00 24.83 2938 O PHE B 506 25.369 81.672 27.859 1.00 25.52 2939 CB PHE B 506 24.496 82.875 25.161 1.00 28.18 2940 CG PHE B 506 23.007 82.842 25.303 1.00 35.33 2941 CD1 PHE B 506 22.245 83.980 25.080 1.00 42.56 2942 CD2 PHE B 506 22.359 81.663 25.657 1.00 40.04 2943 CE1 PHE B 506 20.854 83.940 25.208 1.00 44.70 2944 CE2 PHE B 506 20.977 81.613 25.789 1.00 40.54 2945 CZ PHE B 506 20.223 82.749 25.564 1.00 42.12 2946 N SER B 507 23.961 83.310 28.427 1.00 24.69 2947 CA SER B 507 23.550 82.659 29.674 1.00 24.73 2948 C SER B 507 22.022 82.535 29.745 1.00 26.40 2949 O SER B 507 21.308 83.487 29.491 1.00 25.99 2950 CB SER B 507 24.079 83.449 30.879 1.00 22.19 2951 OC SER B 507 23.653 82.860 32.091 1.00 30.30 2952 N ARG B 508 21.538 81.345 30.091 1.00 26.98 2953 CA ARG B 508 20.104 81.055 30.187 1.00 25.95 2954 C ARG B 508 19.689 80.749 31.637 1.00 24.97 2955 O ARG B 508 20.350 79.979 32.315 1.00 24.35 2956 CB ARG B 508 19.799 79.845 29.310 1.00 21.97 2957 CG ARG B 508 18.365 79.351 29.344 1.00 25.32 2958 CD ARG B 508 18.228 78.126 28.444 1.00 25.67 2959 NE ARG B 508 16.842 77.702 28.312 1.00 36.00 2960 CZ ARG B 508 16.243 76.843 29.128 1.00 36.06 2961 NH1 ARG B 508 16.918 76.307 30.137 1.00 34.19 2962 NH2 ARG B 508 14.967 76.538 28.943 1.00 34.70 2963 N LEU B 509 18.583 81.331 32.099 1.00 26.44 2964 CA LEU B 509 18.121 81.108 33.479 1.00 28.45 2965 C LEU B 509 16.627 80.806 33.560 1.00 28.87 2966 O LEU B 509 15.803 81.707 33.401 1.00 30.99 2967 CB LEU B 509 18.423 82.341 34.342 1.00 27.28 2968 CG LEU B 509 17.867 82.330 35.779 1.00 31.90 2969 CD1 LEU B 509 18.615 81.316 36.647 1.00 29.48 2970 CD2 LEU B 509 18.001 83.714 36.368 1.00 28.89 2971 N GLU B 510 16.277 79.546 33.812 1.00 31.92 2972 CA GLU B 510 14.872 79.152 33.911 1.00 34.67 2973 C GLU B 510 14.310 79.595 35.255 1.00 36.35 2974 O GLU B 510 14.948 79.401 36.288 1.00 34.66 2975 CB GLU B 510 14.725 77.630 33.757 1.00 41.07 2976 CG GLU B 510 15.217 77.090 32.404 1.00 54.35 2977 CD GLU B 510 14.925 75.603 32.189 1.00 58.86 2978 OE1 GLU B 510 15.236 74.789 33.087 1.00 61.22 2979 OE2 GLU B 510 14.393 75.251 31.111 1.00 61.34 2980 N VAL B 511 13.121 80.194 35.248 1.00 36.50 2981 CA VAL B 511 12.531 80.665 36.494 1.00 38.05 2982 C VAL B 511 11.084 80.230 36.692 1.00 42.41 2983 O VAL B 511 10.395 79.856 35.732 1.00 41.92 2984 CB VAL B 511 12.588 82.197 36.592 1.00 31.84 2985 CG1 VAL B 511 14.015 82.673 36.431 1.00 32.42 2986 CG2 VAL B 511 11.687 82.813 35.547 1.00 26.87 2987 N THR B 512 10.633 80.290 37.946 1.00 43.58 2988 CA THR B 512 9.269 79.903 38.292 1.00 48.37 2989 C THR B 512 8.294 80.998 37.899 1.00 50.53 2990 O THR B 512 8.706 82.113 37.584 1.00 51.77 2991 CB THR B 512 9.125 79.644 39.797 1.00 48.57 2992 OC1 THR B 512 9.460 80.834 40.519 1.00 46.96 2993 CG2 THR B 512 10.046 78.515 40.234 1.00 45.82 2994 N ARG B 513 7.002 80.678 37.912 1.00 53.29 2995 CA ARG B 513 5.971 81.648 37.556 1.00 55.54 2996 C ARG B 513 6.043 82.819 38.523 1.00 55.38 2997 O ARG B 513 5.859 83.977 38.138 1.00 55.22 2998 CB ARG B 513 4.582 81.006 37.636 1.00 59.23 2999 CG ARG B 513 3.563 81.601 36.672 1.00 65.98 3000 CD ARG B 513 3.326 83.081 36.916 1.00 74.12 3001 NE ARG B 513 2.773 83.742 35.735 1.00 80.97 3002 CZ ARG B 513 2.403 85.019 35.687 1.00 83.64 3003 NH1 ARG B 513 2.516 85.791 36.760 1.00 86.02 3004 NH2 ARG B 513 1.927 85.528 34.557 1.00 85.44 3005 N ALA B 514 6.315 82.501 39.783 1.00 55.03 3006 CA ALA B 514 6.414 83.504 40.832 1.00 55.46 3007 C ALA B 514 7.496 84.539 40.529 1.00 56.10 3008 O ALA B 514 7.210 85.734 40.426 1.00 56.61 3009 CB ALA B 514 6.692 82.825 42.173 1.00 54.05 3010 N GLU B 515 8.741 84.091 40.388 1.00 55.46 3011 CA GLU B 515 9.819 85.025 40.105 1.00 55.34 3012 C GLU B 515 9.649 85.651 38.729 1.00 54.83 3013 O GLU B 515 10.190 86.723 38.456 1.00 52.33 3014 CB GLU B 515 11.187 84.335 40.232 1.00 57.76 3015 CG GLU B 515 11.221 82.884 39.788 1.00 62.58 3016 CD GLU B 515 12.518 82.184 40.163 1.00 63.27 3017 OE1 GLU B 515 13.035 82.432 41.271 1.00 64.89 3018 OE2 GLU B 515 13.014 81.372 39.359 1.00 66.59 3019 N TRP B 516 8.884 84.992 37.866 1.00 55.79 3020 CA TRP B 516 8.644 85.528 36.534 1.00 57.81 3021 C TRP B 516 7.778 86.782 36.636 1.00 58.51 3022 O TRP B 516 7.778 87.612 35.726 1.00 57.71 3023 CB TRP B 516 7.951 84.499 35.634 1.00 61.48 3024 CG TRP B 516 8.056 84.862 34.187 1.00 66.54 3025 CD1 TRP B 516 9.172 84.777 33.403 1.00 67.26 3026 CD2 TRP B 516 7.039 85.460 33.375 1.00 69.56 3027 NE1 TRP B 516 8.915 85.291 32.154 1.00 71.76 3028 CE2 TRP B 516 7.613 85.718 32.110 1.00 70.88 3029 CE3 TRP B 516 5.700 85.807 33.593 1.00 70.94 3030 CZ2 TRP B 516 6.894 86.308 31.066 1.00 73.50 3031 CZ3 TRP B 516 4.982 86.396 32.552 1.00 74.37 3032 CH2 TRP B 516 5.584 86.639 31.304 1.00 74.71 3033 N GLU B 517 7.047 86.918 37.744 1.00 59.66 3034 CA GLU B 517 6.191 88.085 37.972 1.00 61.72 3035 C GLU B 517 7.035 89.299 38.354 1.00 59.87 3036 O GLU B 517 6.606 90.441 38.196 1.00 58.60 3037 CB GLU B 517 5.182 87.818 39.097 1.00 68.82 3038 CG GLU B 517 4.284 86.612 38.879 1.00 80.60 3039 CD GLU B 517 3.242 86.452 39.976 1.00 87.42 3040 OE1 GLU B 517 3.369 87.128 41.021 1.00 94.80 3041 OE2 GLU B 517 2.301 85.645 39.800 1.00 95.35 3042 N GLN B 518 8.234 89.045 38.867 1.00 57.92 3043 CA GLN B 518 9.132 90.120 39.264 1.00 55.74 3044 C GLN B 518 10.416 90.057 38.436 1.00 54.32 3045 O GLN B 518 11.498 90.393 38.924 1.00 52.85 3046 CB GLN B 518 9.454 90.000 40.745 1.00 54.10 3047 N LYS B 519 10.287 89.646 37.176 1.00 52.69 3048 CA LYS B 519 11.448 89.518 36.309 1.00 52.35 3049 C LYS B 519 12.206 90.819 36.159 1.00 51.69 3050 O LYS B 519 13.397 90.822 35.854 1.00 49.61 3051 CB LYS B 519 11.039 88.983 34.937 1.00 54.31 3052 CG LYS B 519 10.205 89.912 34.088 1.00 55.80 3053 CD LYS B 519 9.723 89.162 32.859 1.00 60.32 3054 CE LYS B 519 8.794 90.002 32.011 1.00 64.05 3055 NZ LYS B 519 8.223 89.191 30.898 1.00 70.92 3056 N ASP B 520 11.511 91.924 36.388 1.00 52.66 3057 CA ASP B 520 12.105 93.251 36.288 1.00 54.22 3058 C ASP B 520 13.209 93.396 37.336 1.00 53.07 3059 O ASP B 520 14.075 94.264 37.229 1.00 52.75 3060 CB ASP B 520 11.032 94.311 36.537 1.00 61.14 3061 CG ASP B 520 9.620 93.779 36.308 1.00 71.19 3062 OD1 ASP B 520 9.300 93.407 35.155 1.00 76.53 3063 OD2 ASP B 520 8.834 93.729 37.283 1.00 72.86 3064 N GLU B 521 13.177 92.533 38.343 1.00 51.01 3065 CA GLU B 521 14.157 92.582 39.416 1.00 50.49 3066 C GLU B 521 15.394 91.714 39.201 1.00 47.73 3067 O GLU B 521 16.372 91.838 39.935 1.00 48.58 3068 CE GLU B 521 13.493 92.200 40.738 1.00 53.54 3069 CG GLU B 521 12.427 93.177 41.199 1.00 60.11 3070 CD GLU B 521 11.705 92.699 42.442 1.00 65.41 3071 OE1 GLU B 521 12.361 92.497 43.486 1.00 67.98 3072 OE2 GLU B 521 10.471 92.521 42.374 1.00 73.58 3073 N PHE B 522 15.359 90.828 38.213 1.00 42.66 3074 CA PHE B 522 16.519 89.985 37.963 1.00 38.90 3075 C PHE B 522 17.583 90.753 37.208 1.00 35.93 3076 O PHE B 522 17.276 91.579 36.345 1.00 38.85 3077 CB PHE B 522 16.122 88.716 37.214 1.00 36.56 3078 CG PHE B 522 15.419 87.710 38.081 1.00 39.04 3079 CD1 PHE B 522 14.106 87.927 38.495 1.00 42.28 3080 CD2 PHE B 522 16.087 86.574 38.539 1.00 36.78 3081 CE1 PHE B 522 13.468 87.029 39.362 1.00 44.30 3082 CE2 PHE B 522 15.461 85.673 39.405 1.00 40.92 3083 CZ PHE B 522 14.146 85.901 39.817 1.00 39.51 3084 N ILE B 523 18.837 90.492 37.555 1.00 31.27 3085 CA ILE B 523 19.959 91.173 36.944 1.00 29.65 3086 C ILE B 523 21.049 90.211 36.483 1.00 29.13 3087 O ILE B 523 21.360 89.236 37.164 1.00 27.36 3088 CB ILE B 523 20.567 92.180 37.937 1.00 34.21 3089 CD1 ILE B 523 19.528 93.251 38.282 1.00 37.38 3090 CG ILE B 523 21.827 92.796 37.364 1.00 34.94 3091 CD1 ILE B 523 19.981 94.227 39.354 1.00 38.56 3092 N CYS B 524 21.610 90.498 35.311 1.00 26.34 3093 CA CYS B 524 22.686 89.699 34.739 1.00 27.10 3094 C CYS B 524 23.946 90.500 34.962 1.00 26.67 3095 O CYS B 524 24.010 91.655 34.569 1.00 27.58 3096 CB CYS B 524 22.473 89.497 33.226 1.00 24.27 3097 SG CYS B 524 23.823 88.626 32.363 1.00 37.60 3098 N ARG B 525 24.951 89.886 35.572 1.00 26.37 3099 CA ARG B 525 26.194 90.576 35.856 1.00 26.35 3100 C ARG B 525 27.419 89.887 35.304 1.00 26.72 3101 O ARG B 525 27.561 88.671 35.400 1.00 29.04 3102 CB ARG B 525 26.376 90.748 37.361 1.00 29.81 3103 CG ARG B 525 27.713 91.393 37.728 1.00 35.40 3104 CD ARG B 525 27.652 92.058 39.099 1.00 46.51 3105 NE ARG B 525 27.796 91.113 40.193 1.00 50.77 3106 CZ ARG B 525 27.461 91.379 41.451 1.00 55.09 3107 NH1 ARG B 525 26.951 92.565 41.763 1.00 54.58 3108 NH2 ARG B 525 27.650 90.464 42.397 1.00 56.77 3109 N ALA B 526 28.311 90.680 34.731 1.00 25.38 3110 CA ALA B 526 29.528 90.142 34.180 1.00 25.38 3111 C ALA B 526 30.721 90.728 34.925 1.00 25.99 3112 O ALA B 526 30.751 91.933 35.210 1.00 25.50 3113 CB ALA B 526 29.629 90.484 32.696 1.00 25.98 3114 N VAL B 527 31.684 89.872 35.259 1.00 23.84 3115 CA VAL B 527 32.895 90.333 35.902 1.00 25.15 3116 C VAL B 527 33.972 90.078 34.880 1.00 26.30 3117 O VAL B 527 34.119 88.958 34.394 1.00 26.20 3118 CB VAL B 527 33.235 89.557 37.177 1.00 24.43 3119 CG1 VAL B 527 34.588 89.990 37.661 1.00 26.95 3120 CG2 VAL B 527 32.191 89.819 38.251 1.00 28.13 3121 N HIS B 528 34.738 91.115 34.569 1.00 26.24 3122 CA HIS B 528 35.772 91.018 33.564 1.00 29.14 3123 C HIS B 528 36.822 92.102 33.805 1.00 31.86 3124 O HIS B 528 36.509 93.216 34.239 1.00 31.05 3125 CB HIS B 528 35.121 91.172 32.179 1.00 29.03 3126 CG HIS B 528 36.077 91.082 31.035 1.00 29.34 3127 ND1 HIS B 528 36.934 92.109 30.696 1.00 33.33 3128 CD2 HIS B 528 36.317 90.090 30.144 1.00 28.93 3129 CE1 HIS B 528 37.655 91.755 29.651 1.00 26.07 3130 NE2 HIS B 528 37.302 90.530 29.295 1.00 32.19 3131 N GLU B 529 38.064 91.757 33.501 1.00 34.08 3132 CA GLU B 529 39.207 92.636 33.676 1.00 39.76 3133 C GLU B 529 39.110 94.037 33.066 1.00 41.50 3134 O GLU B 529 39.410 95.020 33.740 1.00 41.48 3135 CB GLU B 529 40.462 91.959 33.122 1.00 43.03 3136 CG GLU B 529 41.665 92.898 33.086 1.00 56.19 3137 CD GLU B 529 42.827 92.361 32.274 1.00 62.66 3138 OE1 GLU B 529 43.812 93.111 32.093 1.00 63.52 3139 OE2 GLU B 529 42.758 91.198 31.819 1.00 65.43 3140 N ALA B 530 38.703 94.121 31.800 1.00 42.51 3141 CA ALA B 530 38.622 95.399 31.094 1.00 46.03 3142 C ALA B 530 37.495 96.331 31.504 1.00 49.29 3143 O ALA B 530 37.447 97.476 31.056 1.00 50.87 3144 CB ALA B 530 38.557 95.157 29.587 1.00 39.71 3145 N ALA B 531 36.595 95.849 32.352 1.00 52.89 3146 CA ALA B 531 35.467 96.651 32.798 1.00 56.14 3147 C ALA B 531 35.801 97.570 33.976 1.00 59.66 3148 O ALA B 531 35.357 97.342 35.096 1.00 61.00 3149 CB ALA B 531 34.305 95.736 33.162 1.00 52.83 3150 N SER B 532 36.588 98.608 33.730 1.00 63.07 3151 CA SER B 532 36.927 99.544 34.795 1.00 66.03 3152 C SER B 532 35.822 100.594 34.850 1.00 66.08 3153 O SER B 532 35.317 101.031 33.814 1.00 65.35 3154 CB SER B 532 38.270 100.216 34.507 1.00 68.98 3155 OG SER B 532 38.184 101.074 33.384 1.00 74.64 3156 N PRO B 533 35.427 101.019 36.057 1.00 66.51 3157 CA PRO B 533 35.887 100.669 37.404 1.00 65.99 3158 C PRO B 533 35.374 99.349 37.983 1.00 63.48 3159 O PRO B 533 34.327 98.840 37.582 1.00 64.33 3160 CB PRO B 533 35.397 101.843 38.227 1.00 69.06 3161 CG PRO B 533 34.044 102.061 37.629 1.00 71.08 3162 CD PRO B 533 34.358 102.030 36.137 1.00 70.23 3163 N SER B 534 36.134 98.817 38.935 1.00 59.21 3164 CA SER B 534 35.796 97.591 39.648 1.00 55.01 3165 C SER B 534 35.452 96.326 38.852 1.00 50.27 3166 O SER B 534 34.725 95.470 39.347 1.00 48.58 3167 CB SER B 534 34.666 97.894 40.625 1.00 58.20 3168 OG SER B 534 33.587 98.526 39.962 1.00 63.36 3169 N GLN B 535 35.984 96.213 37.639 1.00 44.89 3170 CA GLN B 535 35.771 95.057 36.770 1.00 42.88 3171 C GLN B 535 34.395 94.406 36.823 1.00 41.55 3172 O GLN B 535 34.279 93.181 36.806 1.00 40.80 3173 CB GLN B 535 36.831 93.967 37.020 1.00 37.08 3174 CG GLN B 535 37.869 94.298 38.044 1.00 47.40 3175 CD GLN B 535 38.684 95.499 37.669 1.00 44.36 3176 OE1 GLN B 535 38.862 96.407 38.475 1.00 47.59 3177 NE2 GLN B 535 39.185 95.521 36.436 1.00 54.70 3178 N THR B 536 33.348 95.213 36.874 1.00 39.97 3179 CA THR B 536 32.012 94.650 36.893 1.00 40.62 3180 C THR B 536 31.025 95.487 36.077 1.00 37.57 3181 O THR B 536 31.042 96.707 36.125 1.00 40.85 3182 CB THR B 536 31.508 94.463 38.353 1.00 42.38 3183 OG1 THR B 536 30.112 94.142 38.337 1.00 44.59 3184 CG2 THR B 536 31.730 95.719 39.168 1.00 49.65 3185 N VAL B 537 30.190 94.812 35.299 1.00 35.29 3186 CA VAL B 537 29.182 95.453 34.468 1.00 31.25 3187 C VAL B 537 27.922 94.604 34.563 1.00 29.01 3188 O VAL B 537 27.985 93.382 34.401 1.00 30.11 3189 CB VAL B 537 29.604 95.494 32.983 1.00 34.80 3190 CG1 VAL B 537 28.516 96.148 32.161 1.00 35.52 3191 CG2 VAL B 537 30.888 96.259 32.822 1.00 37.19 3192 N GLN B 538 26.780 95.235 34.808 1.00 26.73 3193 CA GLN B 538 25.533 94.493 34.933 1.00 26.74 3194 C GLN B 538 24.329 95.224 34.368 1.00 27.53 3195 O GLN B 538 24.351 96.431 34.198 1.00 29.89 3196 CB GLN B 538 25.265 94.176 36.400 1.00 28.48 3197 CG GLN B 538 24.976 95.392 37.266 1.00 25.88 3198 CD GLN B 538 24.747 95.005 38.722 1.00 28.51 3199 OE1 GLN B 538 25.498 94.210 39.290 1.00 31.66 3200 NE2 GLN B 538 23.715 95.565 39.328 1.00 27.39 3201 N ARG B 539 23.266 94.487 34.087 1.00 28.05 3202 CA ARG B 539 22.070 95.107 33.565 1.00 30.72 3203 C ARG B 539 20.858 94.312 33.986 1.00 31.33 3204 O ARG B 539 20.897 93.083 34.023 1.00 32.42 3205 CB ARG B 539 22.137 95.180 32.039 1.00 36.30 3206 CG ARG B 539 21.124 96.112 31.414 1.00 45.60 3207 CD ARG B 539 21.771 96.859 30.270 1.00 57.97 3208 NE ARG B 539 23.009 97.482 30.729 1.00 69.46 3209 CZ ARG B 539 23.855 98.147 29.950 1.00 78.18 3210 NH1 ARG B 539 23.604 98.284 28.653 1.00 83.01 3211 NH2 ARG B 539 24.959 98.673 30.470 1.00 81.89 3212 N ALA B 540 19.782 95.022 34.301 1.00 31.92 3213 CA ALA B 540 18.546 94.393 34.717 1.00 34.50 3214 C ALA B 540 17.826 93.909 33.466 1.00 36.68 3215 O ALA B 540 18.068 94.410 32.361 1.00 34.62 3216 CB ALA B 540 17.693 95.391 35.479 1.00 33.91 3217 N VAL B 541 16.974 92.906 33.640 1.00 39.73 3218 CA VAL B 541 16.214 92.346 32.528 1.00 44.47 3219 C VAL B 541 15.351 93.436 31.882 1.00 46.91 3220 O VAL B 541 14.476 94.005 32.527 1.00 44.53 3221 CB VAL B 541 15.305 91.185 33.010 1.00 42.49 3222 CG1 VAL B 541 14.242 90.885 31.970 1.00 47.96 3223 CG2 VAL B 541 16.140 89.945 33.269 1.00 42.43 3224 N SER B 542 15.603 93.731 30.611 1.00 52.25 3225 CA SER B 542 14.829 94.760 29.926 1.00 60.05 3226 C SER B 542 13.426 94.226 29.679 1.00 64.25 3227 O SER B 542 13.247 93.050 29.357 1.00 65.22 3228 CB SER B 542 15.490 95.157 28.600 1.00 60.43 3229 OG SER B 542 15.524 94.070 27.696 1.00 65.30 3230 N VAL B 543 12.432 95.090 29.844 1.00 68.19 3231 CA VAL B 543 11.043 94.694 29.656 1.00 72.45 3232 C VAL B 543 10.277 95.772 28.898 1.00 74.32 3233 O VAL B 543 9.621 96.630 29.497 1.00 75.99 3234 CB VAL B 543 10.353 94.452 31.016 1.00 74.41 3235 CG1 VAL B 543 8.895 94.070 30.801 1.00 76.37 3236 CG2 VAL B 543 11.086 93.367 31.782 1.00 75.78

[0042] Yet another embodiment of the present invention is a 3-D model of a Fc-Cε3/Cε4 region that substantially represents the atomic coordinates specified (i.e., listed) in Table 3. TABLE 3 Atomic coordinates of 1FP5_dimer.pdb with water ATOM ATOM # TYPE RES CHN # X Y Z OCC B 1 N VAL A 336 46.157 62.618 17.991 1.00 58.93 2 CA VAL A 336 45.400 61.812 16.993 1.00 60.44 3 C VAL A 336 44.013 61.427 17.501 1.00 60.07 4 O VAL A 336 43.847 60.389 18.142 1.00 61.48 5 CB VAL A 336 46.155 60.521 16.647 1.00 60.81 6 CG1 VAL A 336 45.464 59.806 15.500 1.00 61.71 7 CG2 VAL A 336 47.590 60.845 16.302 1.00 64.73 8 N SER A 337 43.017 62.257 17.209 1.00 57.95 9 CA SER A 337 41.655 61.983 17.648 1.00 56.60 10 C SER A 337 40.683 61.842 16.476 1.00 55.17 11 O SER A 337 40.981 62.262 15.352 1.00 54.55 12 CB SER A 337 41.185 63.078 18.603 1.00 57.92 13 OG SER A 337 41.489 64.356 18.087 1.00 64.70 14 N ALA A 338 39.527 61.238 16.743 1.00 52.40 15 CA ALA A 338 38.522 61.010 15.711 1.00 50.69 16 C ALA A 338 37.109 61.300 16.192 1.00 50.25 17 O ALA A 338 36.772 61.062 17.354 1.00 51.17 18 CB ALA A 338 38.611 59.573 15.211 1.00 50.21 19 N TYR A 339 36.281 61.808 15.284 1.00 48.22 20 CA TYR A 339 34.899 62.139 15.605 1.00 46.82 21 C TYR A 339 33.990 61.766 14.431 1.00 44.51 22 O TYR A 339 34.372 61.889 13.268 1.00 42.27 23 CB TYR A 339 34.765 63.638 15.915 1.00 50.52 24 CG TYR A 339 35.869 64.198 16.793 1.00 58.40 25 CD1 TYR A 339 37.144 64.445 16.274 1.00 61.23 26 CD2 TYR A 339 35.648 64.456 18.151 1.00 60.99 27 CE1 TYR A 339 38.174 64.929 17.081 1.00 62.71 28 CE2 TYR A 339 36.674 64.943 18.969 1.00 63.53 29 CZ TYR A 339 37.933 65.176 18.427 1.00 64.33 30 OH TYR A 339 38.953 65.644 19.230 1.00 65.07 31 N LEU A 340 32.793 61.291 14.746 1.00 41.90 32 CA LEU A 340 31.831 60.905 13.728 1.00 41.06 33 C LEU A 340 30.571 61.671 14.078 1.00 41.10 34 O LEU A 340 30.136 61.647 15.224 1.00 43.45 35 CB LEU A 340 31.583 59.392 13.779 1.00 36.93 36 CG LEU A 340 30.689 58.770 12.701 1.00 35.91 37 CD1 LEU A 340 31.229 59.100 11.314 1.00 34.60 38 CD2 LEU A 340 30.621 57.264 12.906 1.00 35.51 39 N SER A 341 29.990 62.368 13.108 1.00 39.82 40 CA SER A 341 28.790 63.152 13.385 1.00 39.85 41 C SER A 341 27.598 62.645 12.614 1.00 37.88 42 O SER A 341 27.737 62.076 11.544 1.00 42.10 43 CB SER A 341 29.025 64.627 13.042 1.00 39.34 44 O SER A 341 29.347 64.792 11.672 1.00 44.58 45 N ARG A 342 26.415 62.868 13.158 1.00 36.98 46 CA ARG A 342 25.187 62.437 12.517 1.00 35.20 47 C ARG A 342 24.853 63.417 11.393 1.00 33.18 48 O ARG A 342 25.508 64.443 11.252 1.00 33.16 49 CB ARG A 342 24.070 62.394 13.566 1.00 38.57 50 CG ARG A 342 24.321 61.381 14.689 1.00 39.10 51 CD ARG A 342 23.191 61.364 15.712 1.00 43.21 52 NE ARG A 342 23.231 62.544 16.570 1.00 45.40 53 CZ ARG A 342 24.086 62.714 17.573 1.00 48.22 54 NH1 ARG A 342 24.977 61.777 17.860 1.00 52.78 55 NH2 ARG A 342 24.059 63.831 18.286 1.00 54.34 56 N PRO A 343 23.843 63.112 10.570 1.00 33.03 57 CA PRO A 343 23.497 64.040 9.481 1.00 34.14 58 C PRO A 343 22.907 65.339 10.035 1.00 34.06 59 O PRO A 343 22.302 65.341 11.106 1.00 35.44 60 CB PRO A 343 22.448 63.266 8.667 1.00 33.07 61 CG PRO A 343 22.700 61.811 9.025 1.00 35.06 62 CD PRO A 343 23.029 61.885 10.499 1.00 33.27 63 N SER A 344 23.080 66.445 9.325 1.00 32.17 64 CA SER A 344 22.490 67.691 9.792 1.00 31.75 65 C SER A 344 21.014 67.617 9.414 1.00 32.07 66 O SER A 344 20.660 67.115 8.344 1.00 30.21 67 CB SER A 344 23.144 68.907 9.118 1.00 32.20 68 OG SER A 344 22.665 69.113 7.799 1.00 32.50 69 N PRO A 345 20.127 68.088 10.300 1.00 32.31 70 CA PRO A 345 18.701 68.039 9.975 1.00 30.84 71 C PRO A 345 18.381 68.710 8.629 1.00 29.64 72 O PRO A 345 17.506 68.256 7.891 1.00 30.14 73 CB PRO A 345 18.055 68.741 11.174 1.00 30.96 74 CG PRO A 345 18.941 68.301 12.307 1.00 33.18 75 CD PRO A 345 20.339 68.457 11.713 1.00 33.65 76 N PHE A 346 19.103 69.769 8.292 1.00 28.34 77 CA PHE A 346 18.844 70.447 7.034 1.00 31.46 78 C PHE A 346 19.085 69.522 5.831 1.00 32.46 79 O PHE A 346 18.269 69.465 4.907 1.00 32.59 80 CB PHE A 346 19.711 71.706 6.916 1.00 32.72 81 CG PHE A 346 19.613 72.382 5.579 1.00 36.34 82 CD1 PHE A 346 18.430 72.981 5.172 1.00 40.58 83 CD2 PHE A 346 20.702 72.411 4.722 1.00 36.76 84 CE1 PHE A 346 18.333 73.609 3.933 1.00 38.98 85 CE2 PHE A 346 20.615 73.037 3.482 1.00 40.15 86 CZ PHE A 346 19.425 73.637 3.086 1.00 38.60 87 N ASP A 347 20.203 68.797 5.850 1.00 32.92 88 CA ASP A 347 20.534 67.877 4.764 1.00 33.58 89 C ASP A 347 19.555 66.704 4.733 1.00 34.26 90 O ASP A 347 19.192 66.212 3.666 1.00 32.29 91 CB ASP A 347 21.967 67.349 4.921 1.00 28.72 92 CG ASP A 347 23.008 68.364 4.521 1.00 39.62 93 OD1 ASP A 347 24.225 68.085 4.671 1.00 42.08 94 OD2 ASP A 347 22.609 69.449 4.046 1.00 46.23 95 N LEU A 348 19.120 66.276 5.911 1.00 34.31 96 CA LEU A 348 18.197 65.159 6.036 1.00 37.70 97 C LEU A 348 16.742 65.441 5.629 1.00 38.98 98 O LEU A 348 16.137 64.651 4.902 1.00 38.11 99 CB LEU A 348 18.220 64.641 7.482 1.00 40.66 100 CG LEU A 348 17.333 63.441 7.840 1.00 41.99 101 CD1 LEU A 348 17.738 62.212 7.005 1.00 42.77 102 CD2 LEU A 348 17.476 63.131 9.341 1.00 41.00 103 N PHE A 349 16.183 66.560 6.083 1.00 39.68 104 CA PHE A 349 14.781 66.875 5.794 1.00 42.09 105 C PHE A 349 14.466 67.883 4.695 1.00 45.09 106 O PHE A 349 13.431 67.779 4.038 1.00 48.27 107 CB PHE A 349 14.074 67.328 7.071 1.00 37.36 108 CG PHE A 349 14.189 66.356 8.200 1.00 36.93 109 CD1 PHE A 349 15.021 66.624 9.282 1.00 38.16 110 CD2 PHE A 349 13.487 65.156 8.174 1.00 38.04 111 CE1 PHE A 349 15.155 65.715 10.319 1.00 38.11 112 CE2 PHE A 349 13.614 64.231 9.213 1.00 37.58 113 CZ PHE A 349 14.449 64.511 10.283 1.00 40.39 114 N ILE A 350 15.323 68.874 4.500 1.00 46.66 115 CA ILE A 350 15.052 69.854 3.461 1.00 48.94 116 C ILE A 350 15.695 69.400 2.150 1.00 51.15 117 O ILE A 350 15.007 69.095 1.179 1.00 50.51 118 CB ILE A 350 15.592 71.241 3.860 1.00 48.52 119 CG1 ILE A 350 15.172 71.562 5.299 1.00 49.25 120 CG2 ILE A 350 15.052 72.300 2.923 1.00 49.68 121 CD1 ILE A 350 13.689 71.358 5.567 1.00 46.80 122 N ARG A 351 17.021 69.335 2.155 1.00 52.64 123 CA ARG A 351 17.807 68.931 1.000 1.00 53.76 124 C ARG A 351 17.510 67.486 0.581 1.00 53.61 125 O ARG A 351 17.506 67.164 −0.603 1.00 53.55 126 CB ARG A 351 19.287 69.095 1.341 1.00 56.64 127 CG ARG A 351 20.166 69.584 0.206 1.00 62.18 128 CD ARG A 351 21.225 70.527 0.752 1.00 66.96 129 NE ARG A 351 22.389 70.642 −0.119 1.00 71.13 130 CZ ARG A 351 23.229 69.643 −0.370 1.00 76.72 131 NH1 ARG A 351 23.027 68.455 0.184 1.00 78.73 132 NH2 ARG A 351 24.275 69.829 −1.168 1.00 77.63 133 N LYS A 352 17.253 66.626 1.560 1.00 53.86 134 CA LYS A 352 16.954 65.215 1.312 1.00 54.12 135 C LYS A 352 18.151 64.428 0.772 1.00 52.02 136 O LYS A 352 17.996 63.522 −0.046 1.00 51.77 137 CB LYS A 352 15.775 65.075 0.347 1.00 57.77 138 CG LYS A 352 14.476 65.689 0.846 1.00 62.15 139 CD LYS A 352 13.348 65.439 −0.154 1.00 71.06 140 CE LYS A 352 12.098 66.249 0.171 1.00 74.25 141 NZ LYS A 352 12.293 67.707 −0.085 1.00 78.35 142 N SER A 353 19.342 64.789 1.233 1.00 48.01 143 CA SER A 353 20.568 64.112 0.832 1.00 45.29 144 C SER A 353 21.544 64.154 2.016 1.00 40.67 145 O SER A 353 22.546 64.875 1.994 1.00 40.76 146 CB SER A 353 21.177 64.791 −0.398 1.00 47.97 147 OG SER A 353 21.448 66.155 −0.147 1.00 56.20 148 N PRO A 354 21.244 63.375 3.070 1.00 36.53 149 CA PRO A 354 22.004 63.239 4.319 1.00 32.68 150 C PRO A 354 23.399 62.660 4.139 1.00 31.88 151 O PRO A 354 23.615 61.787 3.302 1.00 29.76 152 CB PRO A 354 21.147 62.294 5.160 1.00 30.29 153 CG PRO A 354 19.799 62.340 4.513 1.00 41.68 154 CD PRO A 354 20.106 62.445 3.065 1.00 33.29 155 N THR A 355 24.342 63.154 4.932 1.00 30.03 156 CA THR A 355 25.704 62.644 4.902 1.00 29.70 157 C THR A 355 26.236 62.578 6.326 1.00 30.82 158 O THR A 355 25.773 63.298 7.213 1.00 30.67 159 CE THR A 355 26.669 63.558 4.136 1.00 32.14 160 OG1 THR A 355 26.806 64.785 4.860 1.00 29.97 161 CG2 THR A 355 26.175 63.837 2.707 1.00 31.76 162 N ILE A 356 27.195 61.693 6.558 1.00 30.53 163 CA ILE A 356 27.816 61.631 7.868 1.00 31.56 164 C ILE A 356 29.279 61.860 7.575 1.00 31.79 165 O ILE A 356 29.752 61.561 6.475 1.00 30.35 166 CB ILE A 356 27.584 60.285 8.583 1.00 30.05 167 CG1 ILE A 356 28.101 59.133 7.729 1.00 31.32 168 CG2 ILE A 356 26.092 60.131 8.890 1.00 31.27 169 CD1 ILE A 356 27.843 57.772 8.337 1.00 36.89 170 N THR A 357 29.995 62.402 8.550 1.00 33.31 171 CA THR A 357 31.395 62.719 8.349 1.00 33.68 172 C THR A 357 32.282 62.197 9.456 1.00 35.47 173 O THR A 357 31.993 62.372 10.641 1.00 36.65 174 CB THR A 357 31.589 64.265 8.245 1.00 33.81 175 OG1 THR A 357 30.917 64.756 7.077 1.00 33.71 176 CG2 THR A 357 33.065 64.632 8.179 1.00 29.63 177 N CYS A 358 33.372 61.566 9.052 1.00 35.41 178 CA CYS A 358 34.346 61.039 9.990 1.00 38.12 179 C CYS A 358 35.507 62.030 9.935 1.00 37.77 180 O CYS A 358 36.127 62.205 8.890 1.00 36.67 181 CB CYS A 358 34.811 59.655 9.532 1.00 40.37 182 SG CYS A 358 35.831 58.729 10.726 1.00 49.83 183 N LEU A 359 35.778 62.691 11.054 1.00 39.77 184 CA LEU A 359 36.853 63.668 11.127 1.00 42.86 185 C LEU A 359 38.007 63.168 11.977 1.00 46.01 186 O LEU A 359 37.831 62.852 13.152 1.00 47.43 187 CB LEU A 359 36.335 64.988 11.711 1.00 42.74 188 CG LEU A 359 37.392 65.996 12.196 1.00 45.03 189 CD1 LEU A 359 38.262 66.448 11.043 1.00 47.59 190 CD2 LEU A 359 36.711 67.197 12.838 1.00 47.51 191 N VAL A 360 39.189 63.107 11.379 1.00 48.26 192 CA VAL A 360 40.380 62.669 12.090 1.00 52.34 193 C VAL A 360 41.357 63.835 12.217 1.00 55.48 194 O VAL A 360 41.672 64.508 11.234 1.00 55.57 195 CB VAL A 360 41.073 61.500 11.353 1.00 53.36 196 CG1 VAL A 360 42.360 61.119 12.071 1.00 51.62 197 CG2 VAL A 360 40.133 60.301 11.284 1.00 51.77 198 N VAL A 361 41.827 64.080 13.435 1.00 58.92 199 CA VAL A 361 42.766 65.167 13.684 1.00 63.13 200 C VAL A 361 44.094 64.607 14.174 1.00 67.77 201 O VAL A 361 44.134 63.862 15.154 1.00 68.38 202 CB VAL A 361 42.223 66.158 14.747 1.00 60.50 203 CG1 VAL A 361 43.245 67.242 15.014 1.00 56.92 204 CG2 VAL A 361 40.929 66.786 14.270 1.00 56.10 205 N ASP A 362 45.174 64.965 13.485 1.00 72.90 206 CA ASP A 362 46.515 64.502 13.841 1.00 78.30 207 C ASP A 362 47.356 65.696 14.284 1.00 81.68 208 O ASP A 362 47.891 66.432 13.452 1.00 81.72 209 CB ASP A 362 47.185 63.829 12.638 1.00 80.22 210 CG ASP A 362 48.444 63.070 13.020 1.00 84.67 211 OD1 ASP A 362 49.122 63.487 13.983 1.00 87.54 212 OD2 ASP A 362 48.763 62.063 12.351 1.00 87.19 213 N LEU A 363 47.474 65.877 15.597 1.00 85.84 214 CA LEU A 363 48.234 66.986 16.165 1.00 89.95 215 C LEU A 363 49.677 67.038 15.672 1.00 92.20 216 O LEU A 363 50.214 68.117 15.432 1.00 92.55 217 CB LEU A 363 48.210 66.906 17.691 1.00 91.66 218 CG LEU A 363 46.823 66.881 18.342 1.00 92.93 219 CD1 LEU A 363 46.976 66.787 19.854 1.00 95.41 220 CD2 LEU A 363 46.049 68.129 17.963 1.00 92.73 221 N ALA A 364 50.304 65.874 15.527 1.00 94.76 222 CA ALA A 364 51.684 65.799 15.049 1.00 97.66 223 C ALA A 364 51.769 64.806 13.890 1.00 99.72 224 O ALA A 364 51.604 63.602 14.079 1.00 100.44 225 GB ALA A 364 52.604 65.365 16.179 1.00 97.99 226 N PRO A 365 52.023 65.303 12.671 1.00 101.15 227 CA PRO A 365 52.116 64.427 11.498 1.00 102.25 228 C PRO A 365 53.437 63.705 11.245 1.00 103.43 229 O PRO A 365 54.497 64.326 11.166 1.00 104.19 230 CB PRO A 365 51.771 65.363 10.339 1.00 101.91 231 CG PRO A 365 50.983 66.479 11.002 1.00 102.27 232 CD PRO A 365 51.767 66.690 12.254 1.00 101.40 233 N SER A 366 53.344 62.385 11.121 1.00 104.18 234 CA SER A 366 54.468 61.512 10.801 1.00 104.43 235 C SER A 366 53.924 61.027 9.463 1.00 104.05 236 O SER A 366 52.736 60.712 9.373 1.00 104.36 237 CB SER A 366 54.545 60.351 11.788 1.00 105.50 238 OG SER A 366 53.377 59.560 11.687 1.00 106.70 239 N LYS A 367 54.739 60.955 8.418 1.00 103.19 240 CA LYS A 367 54.138 60.559 7.156 1.00 102.08 241 C LYS A 367 53.970 59.109 6.733 1.00 100.74 242 O LYS A 367 54.917 58.366 6.460 1.00 101.05 243 CB LYS A 367 54.732 61.364 5.998 1.00 103.30 244 CG LYS A 367 56.216 61.257 5.755 1.00 105.00 245 CD LYS A 367 56.554 62.226 4.633 1.00 104.80 246 CE LYS A 367 57.990 62.133 4.170 1.00 104.70 247 NZ LYS A 367 58.214 63.076 3.034 1.00 105.18 248 N GLY A 368 52.691 58.761 6.678 1.00 98.70 249 CA GLY A 368 52.192 57.464 6.272 1.00 95.62 250 C GLY A 368 50.799 57.900 5.856 1.00 93.12 251 O GLY A 368 50.457 59.062 6.065 1.00 93.17 252 N THR A 369 49.983 57.031 5.277 1.00 90.15 253 CA THR A 369 48.652 57.475 4.880 1.00 86.41 254 C THR A 369 47.623 57.180 5.964 1.00 83.04 255 O THR A 369 47.746 56.198 6.699 1.00 82.54 256 CB THR A 369 48.203 56.808 3.559 1.00 87.73 257 OG1 THR A 369 48.178 55.383 3.721 1.00 88.60 258 CG2 THR A 369 49.157 57.177 2.429 1.00 86.64 259 N VAL A 370 46.620 58.048 6.073 1.00 79.07 260 CA VAL A 370 45.559 57.871 7.058 1.00 74.46 261 C VAL A 370 44.339 57.325 6.332 1.00 72.21 262 O VAL A 370 43.762 57.998 5.482 1.00 71.35 263 CB VAL A 370 45.180 59.199 7.732 1.00 73.33 264 CG1 VAL A 370 44.254 58.933 8.904 1.00 70.92 265 CG2 VAL A 370 46.427 59.926 8.185 1.00 69.77 266 N ASN A 371 43.947 56.102 6.674 1.00 70.13 267 CA ASN A 371 42.809 55.463 6.027 1.00 68.15 268 C ASN A 371 41.521 55.443 6.838 1.00 65.65 269 O ASN A 371 41.533 55.248 8.054 1.00 64.64 270 CB ASN A 371 43.179 54.036 5.631 1.00 70.12 271 CG ASN A 371 44.270 53.995 4.592 1.00 73.56 272 OD1 ASN A 371 44.081 54.447 3.462 1.00 75.10 273 ND2 ASN A 371 45.427 53.463 4.969 1.00 74.76 274 N LEU A 372 40.408 55.651 6.141 1.00 62.66 275 CA LEU A 372 39.088 55.641 6.754 1.00 59.53 276 C LEU A 372 38.226 54.673 5.963 1.00 56.68 277 O LEU A 372 38.071 54.812 4.753 1.00 56.70 278 CB LEU A 372 38.459 57.040 6.728 1.00 59.44 279 CG LEU A 372 39.217 58.172 7.422 1.00 60.55 280 CD1 LEU A 372 38.323 59.386 7.521 1.00 61.28 281 CD2 LEU A 372 39.644 57.739 8.807 1.00 62.83 282 N THR A 373 37.669 53.689 6.654 1.00 53.76 283 CA THR A 373 36.834 52.685 6.015 1.00 51.64 284 C THR A 373 35.420 52.750 6.588 1.00 48.20 285 O THR A 373 35.245 52.799 7.804 1.00 46.65 286 CB THR A 373 37.399 51.275 6.268 1.00 53.15 287 OG1 THR A 373 38.811 51.276 6.027 1.00 57.77 288 CG2 THR A 373 36.729 50.261 5.353 1.00 53.75 289 N THR A 374 34.419 52.749 5.715 1.00 45.34 290 CA THR A 374 33.025 52.801 6.158 1.00 44.94 291 C THR A 374 32.341 51.439 6.059 1.00 43.68 292 O THR A 374 32.636 50.655 5.162 1.00 42.67 293 CB THR A 374 32.209 53.795 5.316 1.00 41.63 294 CG THR A 374 32.623 55.229 5.443 1.00 41.50 295 CD1 THR A 374 33.476 55.912 4.623 1.00 39.67 296 CD2 THR A 374 32.205 56.159 6.452 1.00 35.69 297 NE1 TEP A 374 33.612 57.208 5.059 1.00 35.06 298 CE2 THR A 374 32.844 57.386 6.178 1.00 34.53 299 CE3 THR A 374 31.353 56.072 7.558 1.00 32.37 300 CZ2 THR A 374 32.657 58.521 6.971 1.00 35.43 301 CZ3 THR A 374 31.166 57.199 8.349 1.00 36.11 302 CH2 THR A 374 31.818 58.410 8.050 1.00 37.51 303 N SER A 375 31.421 51.170 6.981 1.00 43.53 304 CA SER A 375 30.666 49.922 6.960 1.00 43.57 305 C SER A 375 29.330 50.089 7.662 1.00 42.59 306 O SER A 375 29.189 50.931 8.550 1.00 43.68 307 CB SER A 375 31.447 48.780 7.626 1.00 45.03 308 OG SER A 375 31.482 48.909 9.034 1.00 45.66 309 N ARG A 376 28.349 49.301 7.234 1.00 40.79 310 CA ARG A 376 27.031 49.321 7.834 1.00 40.12 311 C ARG A 376 26.911 48.102 8.749 1.00 40.59 312 O ARG A 376 27.207 46.982 8.348 1.00 40.90 313 CB ARG A 376 25.947 49.255 6.766 1.00 40.03 314 CG ARG A 376 25.855 50.468 5.863 1.00 43.20 315 CD ARG A 376 24.402 50.717 5.501 1.00 41.05 316 NE ARG A 376 24.120 50.429 4.108 1.00 50.71 317 CZ ARG A 376 22.895 50.300 3.612 1.00 53.97 318 NH1 ARG A 376 21.842 50.428 4.407 1.00 51.88 319 NH2 ARG A 376 22.726 50.058 2.318 1.00 55.55 320 N ALA A 377 26.471 48.319 9.978 1.00 40.20 321 CA ALA A 377 26.327 47.218 10.919 1.00 40.25 322 C ALA A 377 25.470 46.100 10.314 1.00 40.38 323 O ALA A 377 25.621 44.943 10.678 1.00 41.16 324 CB ALA A 377 25.697 47.721 12.222 1.00 33.12 325 N SER A 378 24.585 46.456 9.386 1.00 40.21 326 CA SER A 378 23.697 45.491 8.746 1.00 41.95 327 C SER A 378 24.412 44.694 7.664 1.00 44.92 328 O SER A 378 23.856 43.734 7.134 1.00 44.28 329 CB SER A 378 22.504 46.199 8.108 1.00 40.91 330 OG SER A 378 22.907 46.863 6.920 1.00 40.09 331 N GLY A 379 25.633 45.107 7.332 1.00 46.93 332 CA GLY A 379 26.405 44.419 6.313 1.00 49.77 333 C GLY A 379 26.088 44.884 4.904 1.00 50.60 334 O GLY A 379 26.817 44.576 3.958 1.00 52.95 335 N LYS A 380 24.995 45.626 4.755 1.00 53.72 336 CA LYS A 380 24.612 46.122 3.443 1.00 54.13 337 C LYS A 380 25.689 47.036 2.845 1.00 48.16 338 O LYS A 380 26.592 47.513 3.544 1.00 45.65 339 CB LYS A 380 23.262 46.848 3.517 1.00 62.44 340 CG LYS A 380 22.078 45.908 3.710 1.00 67.72 341 CD LYS A 380 20.748 46.625 3.550 1.00 69.32 342 CE LYS A 380 19.587 45.644 3.619 1.00 73.14 343 NZ LYS A 380 18.267 46.320 3.467 1.00 77.37 344 N PRO A 381 25.614 47.277 1.529 1.00 56.07 345 CA PRO A 381 26.586 48.128 0.835 1.00 56.46 346 C PRO A 381 26.535 49.607 1.225 1.00 54.32 347 O PRO A 381 25.467 50.154 1.511 1.00 56.76 348 CB PRO A 381 26.225 47.936 −0.640 1.00 60.70 349 CG PRO A 381 25.481 46.622 −0.667 1.00 62.01 350 CB PRO A 381 24.655 46.695 0.574 1.00 59.24 351 N VAL A 382 27.701 50.244 1.234 1.00 55.74 352 CA VAL A 382 27.795 51.669 1.531 1.00 55.58 353 C VAL A 382 28.192 52.353 0.220 1.00 55.56 354 O VAL A 382 28.866 51.752 −0.620 1.00 55.22 355 CB VAL A 382 28.874 51.980 2.607 1.00 55.39 356 CG1 VAL A 382 28.592 51.196 3.878 1.00 55.94 357 CG2 VAL A 382 30.261 51.664 2.075 1.00 53.06 358 N ASN A 383 27.773 53.600 0.045 1.00 54.38 359 CA ASN A 383 28.090 54.354 −1.164 1.00 54.63 360 C ASN A 383 29.532 54.843 −1.190 1.00 53.85 361 O ASN A 383 30.303 54.630 −0.254 1.00 52.58 362 CB ASN A 383 27.171 55.566 −1.282 1.00 59.07 363 CG ASN A 383 25.717 55.186 −1.356 1.00 64.60 364 OD1 ASN A 383 24.836 56.024 −1.169 1.00 70.14 365 ND2 ASN A 383 25.450 53.915 −1.638 1.00 71.07 366 N HIS A 384 29.890 55.506 −2.281 1.00 53.46 367 CA HIS A 384 31.229 56.057 −2.426 1.00 52.22 368 C HIS A 384 31.326 57.302 −1.540 1.00 49.10 369 O HIS A 384 30.400 58.105 −1.485 1.00 45.53 370 CB HIS A 384 31.489 56.417 −3.893 1.00 59.11 371 CG HIS A 384 31.676 55.223 −4.778 1.00 62.16 372 ND1 HIS A 384 32.738 54.357 −4.639 1.00 69.15 373 CB2 HIS A 384 30.931 54.745 −5.803 1.00 70.28 374 CE1 HIS A 384 32.640 53.394 −5.539 1.00 75.01 375 NE2 HIS A 384 31.553 53.605 −6.258 1.00 74.58 376 N SER A 385 32.448 57.454 −0.849 1.00 45.07 377 CA SER A 385 32.641 58.583 0.040 1.00 44.61 378 C SER A 385 33.617 59.627 −0.504 1.00 44.58 379 O SER A 385 34.380 59.356 −1.421 1.00 44.21 380 CB SER A 385 33.113 58.076 1.409 1.00 44.61 381 OG SER A 385 34.293 57.290 1.311 1.00 41.13 382 N THR A 386 33.575 60.827 0.065 1.00 44.32 383 CA THR A 386 34.450 61.916 −0.346 1.00 44.35 384 C THR A 386 35.487 62.156 0.737 1.00 44.09 385 O THR A 386 35.149 62.326 1.911 1.00 44.06 386 CB THR A 386 33.664 63.226 −0.580 1.00 45.20 387 OG1 THR A 386 32.744 63.045 −1.662 1.00 51.89 388 CG2 THR A 386 34.616 64.368 −0.936 1.00 47.20 389 N ARG A 387 36.749 62.176 0.326 1.00 44.39 390 CA ARG A 387 37.870 62.378 1.233 1.00 46.68 391 C ARG A 387 38.520 63.763 1.070 1.00 47.05 392 O ARG A 387 38.750 64.228 −0.049 1.00 46.65 393 CB ARG A 387 38.906 61.284 0.979 1.00 48.13 394 CG ARG A 387 40.112 61.330 1.890 1.00 52.77 395 CD ARG A 387 41.247 60.494 1.320 1.00 56.60 396 NE ARG A 387 42.459 60.622 2.121 1.00 60.65 397 CZ ARG A 387 42.705 59.917 3.218 1.00 61.97 398 NH1 ARG A 387 41.821 59.022 3.636 1.00 64.45 399 NH2 ARG A 387 43.819 60.131 3.911 1.00 60.54 400 N LYS A 388 38.820 64.415 2.190 1.00 46.93 401 CA LYS A 388 39.457 65.730 2.167 1.00 47.51 402 C LYS A 388 40.630 65.777 3.143 1.00 48.33 403 O LYS A 388 40.493 65.401 4.306 1.00 46.08 404 CB LYS A 388 38.452 66.823 2.537 1.00 46.64 405 CG LYS A 388 37.274 66.909 1.603 1.00 52.75 406 CD LYS A 388 36.154 67.739 2.195 1.00 58.62 407 CE LYS A 388 34.863 67.538 1.418 1.00 62.49 408 NZ LYS A 388 33.719 68.204 2.101 1.00 67.33 409 N GLU A 389 41.780 66.236 2.651 1.00 50.07 410 CA GLU A 389 42.998 66.357 3.454 1.00 51.86 411 C GLU A 389 43.474 67.807 3.462 1.00 52.81 412 O GLU A 389 43.683 68.408 2.405 1.00 49.21 413 CB GLU A 389 44.106 65.474 2.877 1.00 54.67 414 CG GLU A 389 43.890 63.984 3.056 1.00 65.65 415 CD GLU A 389 44.992 63.159 2.412 1.00 72.66 416 OE1 GLU A 389 46.182 63.449 2.671 1.00 75.92 417 OE2 GLU A 389 44.669 62.220 1.650 1.00 75.78 418 N GLU A 390 43.652 68.371 4.651 1.00 56.06 419 CA GLU A 390 44.100 69.751 4.754 1.00 61.17 420 C GLU A 390 45.146 69.971 5.835 1.00 64.70 421 O GLU A 390 45.002 69.528 6.977 1.00 64.01 422 CB GLU A 390 42.908 70.673 4.993 1.00 64.35 423 CG GLU A 390 43.283 72.121 5.233 1.00 74.80 424 CD GLU A 390 42.091 73.052 5.121 1.00 85.97 425 OE1 GLU A 390 41.053 72.778 5.764 1.00 92.60 426 OE2 GLU A 390 42.197 74.059 4.388 1.00 92.18 427 N LYS A 391 46.204 70.679 5.461 1.00 68.18 428 CA LYS A 391 47.288 70.960 6.388 1.00 71.58 429 C LYS A 391 47.298 72.385 6.920 1.00 76.11 430 O LYS A 391 46.927 73.335 6.231 1.00 75.89 431 CB LYS A 391 48.627 70.654 5.728 1.00 67.28 432 N GLN A 392 47.724 72.508 8.168 1.00 81.85 433 CA GLN A 392 47.854 73.786 8.846 1.00 88.38 434 C GLN A 392 49.118 73.574 9.657 1.00 92.30 435 O GLN A 392 49.100 72.848 10.648 1.00 93.25 436 CB GLN A 392 46.662 74.045 9.777 1.00 85.87 437 CG GLN A 392 45.752 75.178 9.318 1.00 90.76 438 CB GLN A 392 44.727 75.573 10.369 1.00 93.39 439 OE1 GLN A 392 45.076 75.913 11.502 1.00 92.93 440 NE2 GLN A 392 43.453 75.538 9.993 1.00 93.97 441 N ARG A 393 50.221 74.174 9.220 1.00 96.24 442 CA ARG A 393 51.492 74.011 9.916 1.00 100.53 443 C ARG A 393 51.412 74.350 11.403 1.00 102.30 444 O ARG A 393 52.422 74.327 12.107 1.00 101.15 445 CB ARG A 393 52.579 74.853 9.245 1.00 106.99 446 CG ARG A 393 52.404 76.349 9.396 1.00 109.77 447 CB ARG A 393 53.493 77.079 8.636 1.00 115.73 448 NE ARG A 393 53.515 78.505 8.935 1.00 119.73 449 CZ ARG A 393 54.333 79.373 8.350 1.00 121.60 450 NH1 ARG A 393 55.194 78.955 7.430 1.00 121.59 451 NH2 ARG A 393 54.292 80.655 8.684 1.00 121.49 452 N ASN A 394 50.209 74.658 11.876 1.00 103.98 453 CA ASN A 394 50.005 74.970 13.281 1.00 106.60 454 C ASN A 394 50.275 73.682 14.051 1.00 106.89 455 O ASN A 394 51.084 73.650 14.978 1.00 108.55 456 CB ASN A 394 48.564 75.427 13.520 1.00 108.97 457 CG ASN A 394 48.326 75.891 14.947 1.00 112.83 458 OD1 ASN A 394 47.190 76.141 15.348 1.00 114.53 459 ND2 ASN A 394 49.402 76.016 15.719 1.00 114.40 460 N GLY A 395 49.593 72.616 13.648 1.00 105.53 461 CA GLY A 395 49.771 71.331 14.298 1.00 101.15 462 C GLY A 395 48.585 70.423 14.050 1.00 97.82 463 O GLY A 395 48.125 69.721 14.952 1.00 99.41 464 N THR A 396 48.084 70.423 12.822 1.00 94.50 465 CA THR A 396 46.937 69.589 12.522 1.00 89.02 466 C THR A 396 46.763 69.174 11.071 1.00 83.93 467 O THR A 396 46.477 70.000 10.204 1.00 83.27 468 CB THR A 396 45.625 70.278 12.970 1.00 92.03 469 OG1 THR A 396 45.648 70.484 14.388 1.00 94.17 470 CG2 THR A 396 44.414 69.421 12.596 1.00 95.48 471 N LEU A 397 46.942 67.882 10.821 1.00 79.69 472 CA LEU A 397 46.729 67.320 9.500 1.00 74.75 473 C LEU A 397 45.295 66.827 9.604 1.00 71.50 474 O LEU A 397 45.052 65.720 10.081 1.00 74.81 475 CB LEU A 397 47.640 66.120 9.240 1.00 75.72 476 CG LEU A 397 47.188 65.250 8.053 1.00 70.67 477 CB1 LEU A 397 47.668 65.858 6.738 1.00 69.05 478 CB2 LEU A 397 47.723 63.832 8.213 1.00 72.96 479 N THR A 398 44.348 67.659 9.195 1.00 67.61 480 CA THR A 398 42.945 67.286 9.252 1.00 61.30 481 C THR A 398 42.559 66.393 8.076 1.00 56.61 482 O THR A 398 42.960 66.626 6.934 1.00 54.95 483 CB THR A 398 42.044 68.530 9.248 1.00 61.75 484 OG1 THR A 398 42.225 69.255 10.471 1.00 65.40 485 CG2 THR A 398 40.584 68.129 9.108 1.00 63.39 486 N VAL A 399 41.783 65.359 8.371 1.00 51.84 487 CA VAL A 399 41.321 64.437 7.349 1.00 48.05 488 C VAL A 399 39.870 64.085 7.610 1.00 44.81 489 O VAL A 399 39.502 63.689 8.719 1.00 44.41 490 CB VAL A 399 42.132 63.134 7.349 1.00 49.35 491 CG1 VAL A 399 41.590 62.191 6.295 1.00 49.43 492 CG2 VAL A 399 43.594 63.432 7.090 1.00 53.10 493 N THR A 400 39.036 64.246 6.596 1.00 42.44 494 CA THR A 400 37.635 63.909 6.757 1.00 40.44 495 C THR A 400 37.151 63.068 5.602 1.00 38.07 496 O THR A 400 37.692 63.117 4.498 1.00 36.13 497 CB THR A 400 36.731 65.152 6.834 1.00 39.64 498 OG1 THR A 400 36.638 65.755 5.539 1.00 43.72 499 CG2 THR A 400 37.278 66.158 7.822 1.00 38.32 500 N SER A 401 36.140 62.265 5.884 1.00 36.90 501 CA SER A 401 35.531 61.432 4.876 1.00 35.46 502 C SER A 401 34.043 61.612 5.084 1.00 33.95 503 O SER A 401 33.538 61.447 6.192 1.00 34.80 504 CB SER A 401 35.906 59.962 5.060 1.00 36.91 505 OG SER A 401 35.299 59.183 4.040 1.00 40.84 506 N THR A 402 33.352 61.965 4.014 1.00 32.28 507 CA THR A 402 31.928 62.178 4.068 1.00 31.85 508 C THR A 402 31.245 61.092 3.264 1.00 31.76 509 O THR A 402 31.554 60.863 2.090 1.00 30.55 510 CB THR A 402 31.570 63.549 3.505 1.00 31.33 511 OG1 THR A 402 32.284 64.542 4.238 1.00 32.83 512 CG2 THR A 402 30.078 63.818 3.632 1.00 32.70 513 N LEU A 403 30.299 60.433 3.912 1.00 30.72 514 CA LEU A 403 29.582 59.343 3.300 1.00 30.33 515 C LEU A 403 28.115 59.673 3.097 1.00 29.66 516 O LEU A 403 27.415 59.992 4.052 1.00 28.06 517 CB LEU A 403 29.698 58.098 4.187 1.00 28.34 518 CG LEU A 403 28.968 56.831 3.719 1.00 32.10 519 CB1 LEU A 403 29.777 56.175 2.597 1.00 31.94 520 CD2 LEU A 403 28.810 55.844 4.876 1.00 30.42 521 N PRO A 404 27.638 59.617 1.841 1.00 31.48 522 CA PRO A 404 26.233 59.896 1.534 1.00 33.20 523 C PRO A 404 25.451 58.759 2.194 1.00 34.02 524 O PRO A 404 25.845 57.601 2.104 1.00 32.25 525 CB PRO A 404 26.183 59.812 0.010 1.00 33.28 526 CG PRO A 404 27.590 60.165 0.400 1.00 31.82 527 CD PRO A 404 28.413 59.414 0.603 1.00 31.26 528 N VAL A 405 24.362 59.097 2.865 1.00 34.94 529 CA VAL A 405 23.556 58.117 3.564 1.00 38.63 530 C VAL A 405 22.128 58.059 3.032 1.00 40.02 531 O VAL A 405 21.573 59.063 2.598 1.00 40.31 532 CB VAL A 405 23.548 58.457 5.082 1.00 42.09 533 CG1 VAL A 405 22.128 58.490 5.632 1.00 43.95 534 CG2 VAL A 405 24.405 57.456 5.827 1.00 41.76 535 N GLY A 406 21.536 56.872 3.061 1.00 42.35 536 CA GLY A 406 20.168 56.741 2.597 1.00 43.35 537 C GLY A 406 19.246 57.422 3.587 1.00 43.87 538 O GLY A 406 19.446 57.314 4.797 1.00 42.68 539 N THR A 407 18.248 58.134 3.077 1.00 44.40 540 CA THR A 407 17.294 58.840 3.923 1.00 47.37 541 C THR A 407 16.473 57.887 4.778 1.00 48.27 542 O THR A 407 16.392 58.051 5.993 1.00 48.77 543 CB THR A 407 16.312 59.678 3.078 1.00 48.44 544 OG1 THR A 407 17.001 60.791 2.504 1.00 50.00 545 CG2 THR A 407 15.164 60.187 3.938 1.00 53.23 546 N ARG A 408 15.854 56.903 4.130 1.00 48.10 547 CA ARG A 408 15.021 55.935 4.821 1.00 48.54 548 C ARG A 408 15.827 55.060 5.765 1.00 48.48 549 O ARG A 408 15.418 54.831 6.903 1.00 47.34 550 CB ARG A 408 14.275 55.070 3.810 1.00 50.16 551 N ASP A 409 16.966 54.567 5.294 1.00 48.72 552 CA ASP A 409 17.813 53.714 6.121 1.00 50.88 553 C ASP A 409 18.179 54.413 7.426 1.00 49.92 554 O ASP A 409 18.132 53.811 8.502 1.00 49.76 555 CB ASP A 409 19.088 53.340 5.362 1.00 56.18 556 CG ASP A 409 18.799 52.587 4.074 1.00 64.80 557 OD1 ASP A 409 18.118 51.538 4.144 1.00 71.41 558 OD2 ASP A 409 19.247 53.039 2.995 1.00 68.29 559 N TRP A 410 18.533 55.692 7.327 1.00 48.36 560 CA TRP A 410 18.914 56.458 8.503 1.00 46.32 561 C TRP A 410 17.736 56.647 9.447 1.00 46.21 562 O TRP A 410 17.869 56.489 10.660 1.00 44.64 563 CB TRP A 410 19.480 57.826 8.108 1.00 42.82 564 CG TRP A 410 19.890 58.599 9.304 1.00 39.31 565 CD1 TRP A 410 19.133 59.496 9.997 1.00 37.29 566 CD2 TRP A 410 21.093 58.419 10.057 1.00 35.49 567 NE1 TRP A 410 19.781 59.874 11.143 1.00 39.24 568 CE2 TRP A 410 20.987 59.228 11.205 1.00 32.76 569 CE3 TRP A 410 22.249 57.644 9.872 1.00 32.07 570 CZ2 TRP A 410 21.994 59.291 12.176 1.00 29.59 571 CZ3 TRP A 410 23.248 57.704 10.831 1.00 33.68 572 CR2 TRP A 410 23.111 58.527 11.975 1.00 30.56 573 N ILE A 411 16.584 56.989 8.888 1.00 48.11 574 CA ILE A 411 15.391 57.192 9.699 1.00 50.90 575 C ILE A 411 14.951 55.888 10.358 1.00 52.46 576 O ILE A 411 14.371 55.902 11.442 1.00 53.34 577 CB ILE A 411 14.234 57.755 8.854 1.00 51.58 578 CG1 ILE A 411 14.613 59.144 8.330 1.00 52.81 579 CG2 ILE A 411 12.966 57.828 9.685 1.00 51.95 580 CD1 ILE A 411 13.566 59.777 7.431 1.00 59.38 581 N GLU A 412 15.252 54.763 9.715 1.00 53.21 582 CA GLU A 412 14.872 53.463 10.248 1.00 53.12 583 C GLU A 412 15.853 52.919 11.269 1.00 51.24 584 O GLU A 412 15.610 51.864 11.848 1.00 51.40 585 CB GLU A 412 14.691 52.448 9.119 1.00 59.71 586 CG GLU A 412 13.362 52.578 8.383 1.00 70.52 587 CD GLU A 412 13.201 51.540 7.290 1.00 78.58 588 OE1 GLU A 412 13.402 50.338 7.573 1.00 83.44 589 OE2 GLU A 412 12.868 51.924 6.150 1.00 82.10 590 N GLY A 413 16.966 53.618 11.477 1.00 48.47 591 CA GLY A 413 17.923 53.173 12.474 1.00 44.62 592 C GLY A 413 19.213 52.484 12.068 1.00 44.15 593 O GLY A 413 19.882 51.913 12.927 1.00 43.50 594 N GLU A 414 19.588 52.515 10.793 1.00 42.78 595 CA GLU A 414 20.843 51.878 10.406 1.00 40.78 596 C GLU A 414 21.948 52.495 11.249 1.00 39.97 597 O GLU A 414 21.842 53.645 11.690 1.00 37.43 598 CB CLD A 414 21.155 52.111 8.918 1.00 41.96 599 CG GLU A 414 22.519 51.566 8.441 1.00 44.09 600 CD GLU A 414 22.582 50.036 8.360 1.00 49.01 601 OE1 GLU A 414 23.051 49.387 9.325 1.00 46.84 602 OE2 GLU A 414 22.152 49.479 7.327 1.00 49.89 603 N THR A 415 23.001 51.721 11.485 1.00 39.56 604 CA THR A 415 24.136 52.197 12.253 1.00 40.76 605 C THR A 415 25.369 52.113 11.362 1.00 40.07 606 O THR A 415 25.640 51.067 10.777 1.00 42.10 607 CB THR A 415 24.327 51.362 13.544 1.00 44.69 608 OG1 THR A 415 25.707 51.378 13.929 1.00 51.98 609 CG2 THR A 415 23.856 49.948 13.342 1.00 50.00 610 N TYR A 416 26.100 53.220 11.240 1.00 37.57 611 CA TYR A 416 27.282 53.273 10.386 1.00 34.50 612 C TYR A 416 28.549 53.335 11.201 1.00 36.77 613 O TYR A 416 28.562 53.894 12.300 1.00 35.94 614 CB TYR A 416 27.221 54.484 9.466 1.00 34.15 615 CG TYR A 416 26.003 54.515 8.586 1.00 30.65 616 CD1 TYR A 416 24.744 54.823 9.108 1.00 32.53 617 CD2 TYR A 416 26.101 54.211 7.235 1.00 31.72 618 CE1 TYR A 416 23.616 54.828 8.297 1.00 34.27 619 CE2 TYR A 416 24.981 54.210 6.420 1.00 32.11 620 CZ TYR A 416 23.744 54.520 6.956 1.00 33.86 621 OH TYR A 416 22.636 54.518 6.139 1.00 41.22 622 N GLN A 417 29.624 52.771 10.659 1.00 37.58 623 CA GLN A 417 30.878 52.752 11.386 1.00 39.43 624 C GLN A 417 32.062 53.259 10.582 1.00 39.40 625 O GLN A 417 32.227 52.936 9.406 1.00 39.63 626 CB GLN A 417 31.179 51.331 11.889 1.00 41.37 627 CG GLN A 417 32.386 51.250 12.822 1.00 51.81 628 CD GLN A 417 32.744 49.827 13.214 1.00 61.69 629 OE1 CLN A 417 33.229 49.045 12.390 1.00 67.15 630 NE2 CLN A 417 32.504 49.481 14.479 1.00 63.64 631 N CYS A 418 32.888 54.057 11.236 1.00 39.29 632 CA CYS A 418 34.083 54.581 10.611 1.00 41.80 633 C CYS A 418 35.250 53.880 11.282 1.00 42.50 634 O CYS A 418 35.409 53.954 12.500 1.00 43.33 635 CB CYS A 418 34.208 56.099 10.825 1.00 41.95 636 SG CYS A 418 35.696 56.805 10.043 1.00 54.15 637 N ARG A 419 36.049 53.182 10.491 1.00 43.98 638 CA ARG A 419 37.225 52.497 11.007 1.00 47.51 639 C ARG A 419 38.428 53.323 10.558 1.00 48.11 640 O ARG A 419 38.741 53.381 9.370 1.00 47.85 641 CB ARG A 419 37.289 51.068 10.452 1.00 49.08 642 CG ARG A 419 38.642 50.397 10.586 1.00 54.11 643 CD ARG A 419 38.554 48.892 10.304 1.00 64.71 644 NE ARG A 419 39.868 48.275 10.137 1.00 64.09 645 CZ ARG A 419 40.493 48.163 8.968 1.00 70.31 646 NH1 ARG A 419 39.919 48.619 7.861 1.00 68.32 647 NH2 ARG A 419 41.699 47.608 8.905 1.00 71.53 648 N VAL A 420 39.076 53.990 11.508 1.00 51.04 649 CA VAL A 420 40.231 54.824 11.200 1.00 56.22 650 C VAL A 420 41.532 54.039 11.354 1.00 61.25 651 O VAL A 420 41.780 53.422 12.393 1.00 60.11 652 CB VAL A 420 40.295 56.064 12.115 1.00 54.44 653 CG1 VAL A 420 41.494 56.922 11.729 1.00 52.69 654 CG2 VAL A 420 39.003 56.868 12.005 1.00 55.45 655 N THR A 421 42.359 54.071 10.314 1.00 66.23 656 CA THR A 421 43.631 53.356 10.326 1.00 73.18 657 C THR A 421 44.834 54.266 10.130 1.00 76.87 658 O THR A 421 45.157 54.632 9.000 1.00 77.93 659 CB THE A 421 43.671 52.283 9.225 1.00 73.75 660 OG1 THE A 421 42.628 51.328 9.451 1.00 77.71 661 CG2 THE A 421 45.009 51.567 9.227 1.00 75.35 662 N HIS A 422 45.499 54.624 11.226 1.00 81.02 663 CA HIS A 422 46.678 55.483 11.151 1.00 86.07 664 C HIS A 422 47.914 54.596 11.278 1.00 89.67 665 O HIS A 422 47.947 53.680 12.098 1.00 90.00 666 CB HIS A 422 46.660 56.529 12.269 1.00 87.43 667 CG HIS A 422 47.548 57.708 12.008 1.00 90.73 668 ND1 HIS A 422 47.397 58.524 10.909 1.00 93.83 669 CD2 HIS A 422 48.600 58.204 12.704 1.00 91.89 670 CE1 HIS A 422 48.318 59.473 10.936 1.00 94.70 671 NE2 HIS A 422 49.060 59.300 12.015 1.00 93.25 672 N PRO A 423 48.954 54.871 10.474 1.00 92.64 673 CA PRO A 423 50.209 54.111 10.460 1.00 95.19 674 C PRO A 423 50.838 53.628 11.775 1.00 97.06 675 O PRO A 423 51.064 52.431 11.945 1.00 97.57 676 CB PRO A 423 51.155 55.024 9.667 1.00 95.56 677 CG PRO A 423 50.566 56.391 9.853 1.00 93.94 678 CD PRO A 423 49.105 56.112 9.696 1.00 93.12 679 N HIS A 424 51.105 54.542 12.701 1.00 98.71 680 CA HIS A 424 51.769 54.190 13.957 1.00 100.16 681 C HIS A 424 51.021 53.496 15.095 1.00 99.67 682 O HIS A 424 51.609 52.690 15.816 1.00 99.61 683 CB HIS A 424 52.451 55.435 14.522 1.00 102.42 684 CG HIS A 424 53.475 56.022 13.605 1.00 105.47 685 ND1 HIS A 424 53.372 57.298 13.092 1.00 107.10 686 CG2 HIS A 424 54.639 55.521 13.133 1.00 97.46 687 CE1 HIS A 424 54.430 57.556 12.345 1.00 106.81 688 NE2 HIS A 424 55.215 56.494 12.353 1.00 106.61 689 N LEU A 425 49.742 53.798 15.267 1.00 99.19 690 CA LEU A 425 48.972 53.216 16.363 1.00 99.01 691 C LEU A 425 48.692 51.714 16.284 1.00 98.36 692 O LEU A 425 48.479 51.160 15.204 1.00 98.39 693 CB LEU A 425 47.671 53.994 16.507 1.00 100.66 694 CG LEU A 425 47.969 55.495 16.467 1.00 101.95 695 CD1 LEU A 425 46.683 56.285 16.569 1.00 102.59 696 CD2 LEU A 425 48.923 55.856 17.598 1.00 103.85 697 N PRO A 426 48.685 51.038 17.448 1.00 97.57 698 CA PRO A 426 48.435 49.596 17.540 1.00 96.82 699 C PRO A 426 47.075 49.186 16.992 1.00 95.53 700 O PRO A 426 46.990 48.560 15.937 1.00 95.77 701 CB PRO A 426 48.570 49.318 19.037 1.00 97.13 702 CG PRO A 426 48.106 50.605 19.660 1.00 97.88 703 CD PRO A 426 48.802 51.631 18.793 1.00 97.70 704 N ARG A 427 46.015 49.536 17.713 1.00 94.16 705 CA ARG A 427 44.669 49.198 17.274 1.00 92.52 706 C ARG A 427 44.091 50.315 16.408 1.00 89.85 707 O ARG A 427 44.487 51.477 16.517 1.00 89.26 708 CB ARG A 427 43.749 48.948 18.478 1.00 97.34 709 CG ARG A 427 42.381 48.398 18.077 1.00 99.32 710 CD ARG A 427 41.428 48.193 19.253 1.00 105.99 711 NE ARG A 427 40.197 47.532 18.815 1.00 111.10 712 CZ ARG A 427 39.140 47.298 19.588 1.00 111.66 713 NH1 ARG A 427 39.143 47.673 20.861 1.00 111.70 714 NH2 ARG A 427 38.078 46.679 19.087 1.00 110.09 715 N ALA A 428 43.158 49.949 15.538 1.00 86.56 716 CA ALA A 428 42.513 50.910 14.661 1.00 82.70 717 C ALA A 428 41.389 51.602 15.423 1.00 80.03 718 O ALA A 428 40.711 50.981 16.239 1.00 80.29 719 CB ALA A 428 41.953 50.200 13.437 1.00 83.85 720 N LEU A 429 41.203 52.892 15.164 1.00 76.76 721 CA LEU A 429 40.144 53.651 15.815 1.00 72.72 722 C LEU A 429 38.820 53.289 15.164 1.00 69.67 723 O LEU A 429 38.742 53.128 13.947 1.00 68.64 724 CB LEU A 429 40.392 55.156 15.671 1.00 73.60 725 CG LEU A 429 41.169 55.847 16.793 1.00 73.35 726 CD1 LEU A 429 41.498 57.280 16.404 1.00 72.09 727 CD2 LEU A 429 40.333 55.813 18.065 1.00 76.40 728 N MET A 430 37.779 53.153 15.976 1.00 66.83 729 CA MET A 430 36.468 52.814 15.449 1.00 64.81 730 C MET A 430 35.384 53.678 16.074 1.00 61.41 731 O MET A 430 35.274 53.776 17.299 1.00 60.84 732 CB MET A 430 36.173 51.335 15.691 1.00 68.22 733 CG MET A 430 37.247 50.416 15.133 1.00 74.39 734 SD MET A 430 36.886 48.679 15.387 1.00 83.18 735 CE MET A 430 36.836 48.607 17.194 1.00 84.12 736 N ARG A 431 34.590 54.312 15.218 1.00 57.17 737 CA ARG A 431 33.506 55.172 15.674 1.00 54.04 738 C ARG A 431 32.234 54.752 14.963 1.00 50.58 739 O ARG A 431 32.270 54.367 13.796 1.00 50.46 740 CB ARG A 431 33.825 56.641 15.364 1.00 55.16 741 CG ARG A 431 35.036 57.187 16.109 1.00 59.24 742 CD ARG A 431 34.802 57.172 17.611 1.00 63.93 743 NE ARG A 431 35.983 57.586 18.363 1.00 70.30 744 CZ ARG A 431 36.070 57.557 19.689 1.00 76.24 745 NH1 ARG A 431 35.041 57.131 20.417 1.00 77.83 746 NH2 ARG A 431 37.185 57.952 20.289 1.00 77.12 747 N SER A 432 31.112 54.812 15.669 1.00 46.92 748 CA SER A 432 29.835 54.437 15.084 1.00 45.15 749 C SER A 432 28.784 55.482 15.398 1.00 42.49 750 O SER A 432 28.901 56.218 16.379 1.00 42.76 751 CB SER A 432 29.394 53.068 15.610 1.00 44.31 752 OG SER A 432 29.316 53.084 17.018 1.00 49.96 753 N THR A 433 27.749 55.540 14.570 1.00 40.28 754 CA THR A 433 26.691 56.522 14.763 1.00 39.71 755 C THR A 433 25.356 55.996 14.257 1.00 39.49 756 O THR A 433 25.315 55.186 13.334 1.00 40.22 757 CB THR A 433 27.023 57.839 14.022 1.00 38.07 758 OG1 THR A 433 26.006 58.807 14.295 1.00 39.56 759 CG2 THR A 433 27.088 57.609 12.518 1.00 36.99 760 N THR A 434 24.272 56.461 14.874 1.00 39.18 761 CA THR A 434 22.913 56.068 14.512 1.00 40.70 762 C THR A 434 21.965 57.186 14.934 1.00 40.23 763 O THR A 434 22.364 58.091 15.659 1.00 41.18 764 CB THR A 434 22.484 54.784 15.256 1.00 43.01 765 OG1 THR A 434 22.362 55.052 16.661 1.00 47.85 766 CG2 THR A 434 23.524 53.726 15.105 1.00 48.67 767 N LYS A 435 20.714 57.125 14.496 1.00 40.97 768 CA LYS A 435 19.767 58.150 14.889 1.00 45.73 769 C LYS A 435 19.601 58.021 16.398 1.00 48.93 770 O LYS A 435 19.710 56.930 16.942 1.00 48.49 771 CB LYS A 435 18.434 57.937 14.194 1.00 45.94 772 N THR A 436 19.365 59.133 17.082 1.00 52.01 773 CA THR A 436 19.171 59.080 18.526 1.00 54.88 774 C THR A 436 17.722 58.684 18.774 1.00 55.70 775 O THR A 436 16.823 59.146 18.077 1.00 55.21 776 CB THR A 436 19.438 60.454 19.191 1.00 56.24 777 OG1 THR A 436 20.821 60.802 19.038 1.00 60.56 778 CG2 THR A 436 19.090 60.412 20.677 1.00 57.04 779 N SER A 437 17.501 57.810 19.748 1.00 57.93 780 CA SER A 437 16.149 57.380 20.080 1.00 60.42 781 C SER A 437 15.683 58.239 21.249 1.00 60.49 782 O SER A 437 16.357 59.203 21.623 1.00 60.21 783 CB SER A 437 16.133 55.894 20.470 1.00 61.57 784 OG SER A 437 16.957 55.651 21.600 1.00 65.51 785 N GLY A 438 14.533 57.895 21.821 1.00 60.09 786 CA GLY A 438 14.022 58.666 22.939 1.00 58.42 787 C GLY A 438 12.937 59.630 22.511 1.00 57.80 788 O GLY A 438 12.648 59.747 21.322 1.00 56.51 789 N PRO A 439 12.309 60.333 23.467 1.00 57.81 790 CA PRO A 439 11.242 61.295 23.185 1.00 56.19 791 C PRO A 439 11.692 62.422 22.263 1.00 53.91 792 O PRO A 439 12.886 62.709 22.147 1.00 53.91 793 CB PRO A 439 10.865 61.806 24.576 1.00 57.79 794 CG PRO A 439 11.147 60.633 25.448 1.00 58.60 795 CD PRO A 439 12.485 60.173 24.921 1.00 60.65 796 N ARG A 440 10.722 63.055 21.612 1.00 51.09 797 CA ARG A 440 10.990 64.163 20.702 1.00 48.90 798 C ARG A 440 10.220 65.365 21.231 1.00 45.83 799 O ARG A 440 9.188 65.202 21.881 1.00 45.88 800 CB ARG A 440 10.501 63.836 19.289 1.00 49.95 801 CG ARG A 440 10.919 62.473 18.771 1.00 59.03 802 CB ARG A 440 12.406 62.373 18.448 1.00 65.31 803 NE ARG A 440 12.814 60.973 18.342 1.00 72.31 804 CZ ARG A 440 13.986 60.553 17.878 1.00 74.99 805 NH1 ARG A 440 14.894 61.419 17.460 1.00 77.22 806 NE2 ARG A 440 14.252 59.255 17.837 1.00 78.59 807 N ALA A 441 10.727 66.564 20.957 1.00 42.09 808 CA ALA A 441 10.079 67.800 21.387 1.00 39.26 809 C ALA A 441 10.476 68.894 20.413 1.00 38.22 810 O ALA A 441 11.649 69.034 20.076 1.00 38.95 811 CB ALA A 441 10.511 68.170 22.798 1.00 36.56 812 N ALA A 442 9.496 69.666 19.966 1.00 37.22 813 CA ALA A 442 9.739 70.729 19.011 1.00 37.60 814 C ALA A 442 10.550 71.879 19.590 1.00 38.65 815 O ALA A 442 10.553 72.103 20.798 1.00 40.22 816 CB ALA A 442 8.415 71.248 18.481 1.00 37.17 817 N PRO A 443 11.260 72.619 18.722 1.00 38.04 818 CA PRO A 443 12.089 73.765 19.104 1.00 36.79 819 C PRO A 443 11.224 75.019 19.243 1.00 38.14 820 O PRO A 443 10.236 75.174 18.521 1.00 37.39 821 CB PRO A 443 13.050 73.923 17.921 1.00 36.30 822 CG PRO A 443 12.946 72.632 17.159 1.00 36.35 823 CD PRO A 443 11.512 72.249 17.320 1.00 37.85 824 N GLU A 444 11.594 75.894 20.173 1.00 36.28 825 CA GLU A 444 10.901 77.163 20.371 1.00 35.57 826 C GLU A 444 11.941 78.171 19.888 1.00 33.87 827 O GLU A 444 13.110 78.105 20.291 1.00 33.43 828 CB GLU A 444 10.580 77.383 21.851 1.00 38.68 829 N VAL A 445 11.520 79.097 19.033 1.00 30.18 830 CA VAL A 445 12.432 80.070 18.450 1.00 28.24 831 C VAL A 445 12.136 81.523 18.811 1.00 28.44 832 O VAL A 445 11.000 81.975 18.721 1.00 26.78 833 CB VAL A 445 12.417 79.937 16.905 1.00 28.10 834 CG1 VAL A 445 13.370 80.933 16.274 1.00 25.56 835 CG2 VAL A 445 12.771 78.521 16.511 1.00 26.30 836 N TYR A 446 13.175 82.251 19.203 1.00 27.87 837 CA TYR A 446 13.019 83.651 19.551 1.00 27.91 838 C TYR A 446 14.193 84.460 19.024 1.00 27.06 839 O TYR A 446 15.326 84.307 19.480 1.00 27.96 840 CB TYR A 446 12.898 83.836 21.074 1.00 26.45 841 CG TYR A 446 12.749 85.289 21.447 1.00 26.59 842 CD1 TYR A 446 11.714 86.057 20.905 1.00 28.48 843 CD2 TYR A 446 13.659 85.914 22.305 1.00 29.02 844 CE1 TYR A 446 11.589 87.417 21.204 1.00 33.24 845 CE2 TYR A 446 13.543 87.274 22.616 1.00 31.33 846 CZ TYR A 446 12.506 88.015 22.059 1.00 36.01 847 OH TYR A 446 12.387 89.352 22.338 1.00 36.54 848 N ALA A 447 13.914 85.326 18.060 1.00 28.07 849 CA ALA A 447 14.949 86.150 17.439 1.00 27.67 850 C ALA A 447 14.815 87.579 17.932 1.00 29.19 851 O ALA A 447 13.702 88.036 18.173 1.00 31.10 852 CB ALA A 447 14.802 86.098 15.931 1.00 23.97 853 N PHE A 448 15.929 88.293 18.079 1.00 29.56 854 CA PHE A 448 15.849 89.657 18.578 1.00 32.50 855 C PHE A 448 17.075 90.483 18.246 1.00 33.67 856 O PHE A 448 18.112 89.950 17.872 1.00 35.26 857 CB PHE A 448 15.659 89.630 20.097 1.00 35.29 858 CG PHE A 448 16.849 89.077 20.838 1.00 37.04 859 CB1 PHE A 448 17.912 89.909 21.195 1.00 36.66 860 CD2 PHE A 448 16.934 87.714 21.127 1.00 34.95 861 CE1 PHE A 448 19.049 89.382 21.824 1.00 40.91 862 CE2 PHE A 448 18.066 87.178 21.753 1.00 35.99 863 CZ PHE A 448 19.123 88.014 22.103 1.00 35.15 864 N ALA A 449 16.952 91.796 18.396 1.00 35.81 865 CA ALA A 449 18.066 92.693 18.131 1.00 37.63 866 C ALA A 449 18.617 93.253 19.438 1.00 40.96 867 O ALA A 449 17.885 93.441 20.403 1.00 40.14 868 CB ALA A 449 17.623 93.831 17.230 1.00 33.60 869 N THR A 450 19.918 93.509 19.448 1.00 45.40 870 CA THR A 450 20.606 94.071 20.595 1.00 50.82 871 C THR A 450 20.515 95.597 20.498 1.00 53.78 872 O THR A 450 20.673 96.169 19.417 1.00 54.14 873 CB THR A 450 22.090 93.665 20.587 1.00 51.45 874 OG1 THR A 450 22.192 92.242 20.450 1.00 54.12 875 CG2 THR A 450 22.769 94.093 21.877 1.00 55.58 876 N PRO A 451 20.260 96.275 21.626 1.00 56.74 877 CA PRO A 451 20.157 97.737 21.623 1.00 59.05 878 C PRO A 451 21.427 98.391 21.080 1.00 61.00 879 O PRO A 451 22.535 98.080 21.521 1.00 59.71 880 CB PRO A 451 19.933 98.073 23.098 1.00 60.52 881 CG PRO A 451 19.262 96.851 23.640 1.00 61.14 882 CD PRO A 451 20.049 95.739 22.981 1.00 59.39 883 N GLU A 452 21.272 99.285 20.112 1.00 64.30 884 CA GLU A 452 22.428 99.975 19.558 1.00 69.17 885 C GLU A 452 22.252 101.463 19.842 1.00 72.61 886 O GLU A 452 21.667 102.206 19.057 1.00 73.59 887 CB GLU A 452 22.560 99.712 18.054 1.00 65.66 888 CG GLU A 452 24.015 99.566 17.577 1.00 61.46 889 CD GLU A 452 24.717 98.317 18.133 1.00 60.52 890 OE1 GLU A 452 24.053 97.264 18.251 1.00 63.47 891 OE2 GLU A 452 25.934 98.373 18.433 1.00 53.34 892 N THR A 453 22.763 101.869 20.997 1.00 76.75 893 CA THR A 453 22.693 103.242 21.481 1.00 81.00 894 C THR A 453 23.886 104.027 20.913 1.00 82.30 895 O THR A 453 25.038 103.710 21.215 1.00 82.08 896 CB THR A 453 22.737 103.191 23.010 1.00 85.65 897 CG THR A 453 22.182 104.367 23.734 1.00 89.76 898 CD1 THR A 453 20.939 104.921 23.588 1.00 92.34 899 CD2 THR A 453 22.819 105.083 24.795 1.00 94.15 900 NH1 THR A 453 20.764 105.934 24.502 1.00 94.99 901 CE2 THR A 453 21.904 106.055 25.255 1.00 95.56 902 CE3 THR A 453 24.079 104.995 25.407 1.00 95.36 903 CZ2 THR A 453 22.208 106.935 26.300 1.00 97.14 904 CZ3 THR A 453 24.380 105.869 26.445 1.00 95.61 905 CH2 THR A 453 23.447 106.826 26.880 1.00 97.12 906 N PRO A 454 23.619 105.058 20.080 1.00 84.10 907 CA PRO A 454 24.606 105.931 19.422 1.00 87.24 908 C PRO A 454 25.892 106.316 20.162 1.00 90.52 909 O PRO A 454 26.088 105.978 21.333 1.00 89.75 910 CB PRO A 454 23.775 107.150 18.988 1.00 84.91 911 CG PRO A 454 22.475 107.017 19.740 1.00 83.62 912 CD PRO A 454 22.259 105.537 19.793 1.00 84.60 913 N GLY A 455 26.751 107.055 19.464 1.00 91.72 914 CA GLY A 455 28.048 107.413 20.012 1.00 94.13 915 C GLY A 455 28.730 106.132 19.601 1.00 96.28 916 O GLY A 455 28.613 105.125 20.301 1.00 97.74 917 N SER A 456 29.442 106.142 18.478 1.00 99.11 918 CA SER A 456 29.974 104.869 18.023 1.00 96.15 919 C SER A 456 31.407 104.465 17.676 1.00 91.50 920 O SER A 456 32.292 105.284 17.333 1.00 88.52 921 CB SER A 456 29.092 104.378 16.879 1.00 95.05 922 OG SER A 456 28.910 105.375 15.884 1.00 110.76 923 N ARG A 457 31.541 103.136 17.752 1.00 87.73 924 CA ARG A 457 32.664 102.251 17.520 1.00 87.81 925 C ARG A 457 31.678 101.103 17.647 1.00 86.30 926 O ARG A 457 31.026 100.998 18.697 1.00 90.57 927 CB ARG A 457 33.634 102.261 18.675 1.00 94.67 928 N ASP A 458 31.512 100.259 16.627 1.00 87.32 929 CA ASP A 458 30.441 99.286 16.780 1.00 80.43 930 C ASP A 458 30.422 97.963 16.080 1.00 72.83 931 O ASP A 458 31.410 97.437 15.599 1.00 73.96 932 CB ASP A 458 29.150 99.985 16.385 1.00 83.19 933 CG ASP A 458 29.102 100.300 14.890 1.00 85.09 934 OD1 ASP A 458 30.065 100.906 14.378 1.00 91.25 935 OD2 ASP A 458 28.108 99.939 14.217 1.00 90.84 936 N LYS A 459 29.196 97.451 16.076 1.00 66.05 937 CA LYS A 459 28.782 96.211 15.437 1.00 61.75 938 C LYS A 459 27.368 95.983 15.886 1.00 56.14 939 O LYS A 459 27.144 95.648 17.046 1.00 56.54 940 CB LYS A 459 29.641 95.031 15.889 1.00 68.18 941 CG LYS A 459 30.801 94.804 14.969 1.00 71.85 942 CD LYS A 459 30.406 94.863 13.499 1.00 73.79 943 CE LYS A 459 31.655 94.839 12.626 1.00 76.14 944 NZ LYS A 459 31.341 94.675 11.169 1.00 79.35 945 N ARG A 460 26.406 96.194 15.001 1.00 52.32 946 CA ARG A 460 25.035 95.951 15.377 1.00 47.59 947 C ARG A 460 24.860 94.436 15.290 1.00 43.34 948 O ARG A 460 25.477 93.761 14.462 1.00 40.40 949 CB ARG A 460 24.104 96.726 14.456 1.00 49.27 950 CG ARG A 460 24.275 98.216 14.671 1.00 56.23 951 CD ARG A 460 23.659 99.006 13.532 1.00 63.20 952 NE ARG A 460 23.997 100.426 13.596 1.00 68.02 953 CZ ARG A 460 25.145 100.955 13.180 1.00 70.46 954 NH1 ARG A 460 26.094 100.185 12.656 1.00 72.23 955 NH2 ARG A 460 25.336 102.264 13.285 1.00 73.53 956 N THR A 461 24.062 93.910 16.198 1.00 39.19 957 CA THR A 461 23.879 92.474 16.278 1.00 36.81 958 C THR A 461 22.447 92.004 16.401 1.00 34.03 959 O THR A 461 21.631 92.607 17.110 1.00 33.96 960 CB THR A 461 24.603 91.890 17.512 1.00 39.13 961 OG1 THR A 461 25.957 92.357 17.557 1.00 46.04 962 CG2 THR A 461 24.630 90.380 17.421 1.00 45.48 963 N LEU A 462 22.157 90.904 15.714 1.00 29.84 964 CA LEU A 462 20.853 90.267 15.788 1.00 28.03 965 C LEU A 462 21.205 88.926 16.410 1.00 27.33 966 O LEU A 462 22.307 88.414 16.207 1.00 24.47 967 CE LEU A 462 20.223 90.074 14.403 1.00 25.97 968 CG LEU A 462 19.888 91.362 13.635 1.00 33.39 969 CD1 LEU A 462 19.172 91.007 12.319 1.00 32.36 970 CD2 LEU A 462 19.014 92.263 14.483 1.00 30.72 971 N ALA A 463 20.286 88.359 17.178 1.00 25.83 972 CA ALA A 463 20.577 87.111 17.836 1.00 25.65 973 C ALA A 463 19.330 86.279 17.957 1.00 26.32 974 O ALA A 463 18.214 86.790 17.846 1.00 27.53 975 CB ALA A 463 21.179 87.381 19.212 1.00 28.15 976 N CYS A 464 19.518 84.992 18.195 1.00 21.23 977 CA CYS A 464 18.388 84.093 18.276 1.00 24.77 978 C CYS A 464 18.599 83.016 19.314 1.00 22.14 979 O CYS A 464 19.683 82.431 19.402 1.00 24.66 980 CB CYS A 464 18.193 83.429 16.914 1.00 22.04 981 SG CYS A 464 16.790 82.298 16.720 1.00 34.06 982 N LEU A 465 17.548 82.741 20.075 1.00 22.44 983 CA LEU A 465 17.598 81.697 21.089 1.00 23.11 984 C LEU A 465 16.644 80.615 20.641 1.00 22.43 985 O LEU A 465 15.483 80.898 20.352 1.00 23.73 986 CB LEU A 465 17.155 82.230 22.461 1.00 22.99 987 CG LEU A 465 16.810 81.177 23.538 1.00 19.04 988 CD1 LEU A 465 18.035 80.331 23.866 1.00 21.72 989 CD2 LEU A 465 16.347 81.884 24.818 1.00 28.23 990 N ILE A 466 17.125 79.380 20.581 1.00 22.56 991 CA ILE A 466 16.277 78.268 20.169 1.00 22.11 992 C ILE A 466 16.302 77.256 21.297 1.00 24.25 993 O ILE A 466 17.375 76.815 21.706 1.00 24.93 994 CB ILE A 466 16.781 77.654 18.861 1.00 22.15 995 CG1 TLE A 466 16.849 78.750 17.786 1.00 23.07 996 CG2 ILE A 466 15.822 76.525 18.416 1.00 25.24 997 CD1 ILE A 466 17.509 78.318 16.496 1.00 33.12 998 N GLN A 467 15.132 76.863 21.793 1.00 24.63 999 CA GLN A 467 15.120 75.970 22.951 1.00 28.64 1000 C GLN A 467 13.982 74.963 23.072 1.00 31.08 1001 O GLN A 467 13.071 74.915 22.235 1.00 31.00 1002 CB GLN A 467 15.172 76.830 24.228 1.00 25.58 1003 CG GLN A 467 13.943 77.727 24.404 1.00 25.53 1004 CD GLN A 467 14.044 78.693 25.599 1.00 30.72 1005 OE1 GLN A 467 14.790 78.456 26.549 1.00 29.76 1006 NE2 GLN A 467 13.273 79.779 25.550 1.00 32.18 1007 N ASN A 468 14.083 74.147 24.123 1.00 33.71 1008 CA ASN A 468 13.114 73.106 24.459 1.00 36.96 1009 C ASN A 468 12.993 71.999 23.423 1.00 38.20 1010 O ASN A 468 11.931 71.392 23.288 1.00 38.39 1011 CB ASN A 468 11.731 73.719 24.676 1.00 41.06 1012 CG ASN A 468 11.748 74.837 25.686 1.00 46.41 1013 OD1 ASN A 468 12.372 74.721 26.741 1.00 50.82 1014 ND2 ASN A 468 11.052 75.928 25.376 1.00 53.31 1015 N PHE A 469 14.065 71.732 22.685 1.00 35.74 1016 CA PHE A 469 14.003 70.690 21.677 1.00 33.87 1017 C PHE A 469 14.804 69.453 22.056 1.00 33.63 1018 O PHE A 469 15.727 69.513 22.860 1.00 34.78 1019 CB PHE A 469 14.495 71.228 20.322 1.00 29.12 1020 CG PHE A 469 15.926 71.691 20.334 1.00 26.27 1021 CB1 PHE A 469 16.959 70.792 20.133 1.00 22.45 1022 CD2 PHE A 469 16.238 73.034 20.539 1.00 22.06 1023 CE1 PHE A 469 18.285 71.214 20.126 1.00 23.84 1024 CE2 PHE A 469 17.564 73.465 20.536 1.00 28.02 1025 CZ PHE A 469 18.593 72.549 20.327 1.00 23.33 1026 N MET A 470 14.431 68.327 21.466 1.00 35.64 1027 CA MET A 470 15.120 67.065 21.687 1.00 37.62 1028 C MET A 470 14.684 66.104 20.596 1.00 36.36 1029 O MET A 470 13.529 66.122 20.177 1.00 36.33 1030 CB MET A 470 14.804 66.495 23.076 1.00 42.61 1031 CG MET A 470 13.354 66.179 23.350 1.00 50.60 1032 SD MET A 470 13.141 65.744 25.113 1.00 66.08 1033 CE MET A 470 13.780 64.056 25.134 1.00 66.35 1034 N PRO A 471 15.613 65.283 20.079 1.00 34.63 1035 CA PRO A 471 17.039 65.169 20.418 1.00 32.61 1036 C PRO A 471 17.818 66.453 20.143 1.00 31.92 1037 O PRO A 471 17.244 67.436 19.685 1.00 29.59 1038 CE PRO A 471 17.520 64.015 19.538 1.00 33.95 1039 CG PRO A 471 16.277 63.227 19.295 1.00 37.90 1040 CB PRO A 471 15.246 64.291 19.058 1.00 34.78 1041 N GLU A 472 19.128 66.413 20.386 1.00 32.28 1042 CA GLU A 472 20.001 67.580 20.234 1.00 36.49 1043 C GLU A 472 20.380 68.043 18.830 1.00 35.52 1044 O GLU A 472 20.870 69.162 18.683 1.00 34.87 1045 CB GLU A 472 21.302 67.377 21.015 1.00 41.97 1046 CG GLU A 472 22.213 66.306 20.423 1.00 54.78 1047 CD GLU A 472 23.527 66.144 21.184 1.00 62.41 1048 OE1 GLU A 472 23.603 66.579 22.356 1.00 67.26 1049 OE2 GLU A 472 24.481 65.566 20.613 1.00 64.96 1050 N ASP A 473 20.161 67.221 17.805 1.00 34.38 1051 CA ASP A 473 20.543 67.629 16.452 1.00 31.83 1052 C ASP A 473 19.602 68.686 15.886 1.00 31.24 1053 O ASP A 473 18.380 68.528 15.901 1.00 31.80 1054 CB ASP A 473 20.621 66.420 15.516 1.00 34.73 1055 CG ASP A 473 21.746 65.453 15.904 1.00 40.83 1056 OD1 ASP A 473 22.841 65.924 16.296 1.00 44.18 1057 OD2 ASP A 473 21.539 64.222 15.810 1.00 40.17 1058 N ILE A 474 20.184 69.774 15.398 1.00 26.96 1059 CA ILE A 474 19.393 70.856 14.854 1.00 25.39 1060 C ILE A 474 20.225 71.715 13.892 1.00 24.74 1061 O ILE A 474 21.436 71.824 14.031 1.00 25.20 1062 CB ILE A 474 18.842 71.738 16.008 1.00 23.81 1063 CG1 ILE A 474 17.748 72.675 15.502 1.00 22.23 1064 CG2 ILE A 474 19.974 72.538 16.647 1.00 27.10 1065 CD1 ILE A 474 17.064 73.456 16.650 1.00 25.30 1066 N SER A 475 19.570 72.288 12.891 1.00 23.27 1067 CA SER A 475 20.252 73.170 11.952 1.00 22.17 1068 C SER A 475 19.609 74.534 12.148 1.00 21.71 1069 O SER A 475 18.393 74.649 12.224 1.00 20.84 1070 CB SER A 475 20.049 72.721 10.507 1.00 20.43 1071 OG SER A 475 20.589 71.436 10.294 1.00 30.00 1072 N VAL A 476 20.442 75.558 12.213 1.00 21.76 1073 CA VAL A 476 19.980 76.906 12.425 1.00 21.72 1074 C VAL A 476 20.435 77.725 11.249 1.00 23.56 1075 O VAL A 476 21.555 77.564 10.780 1.00 25.95 1076 CB VAL A 476 20.606 77.513 13.715 1.00 21.56 1077 CG1 VAL A 476 20.157 78.975 13.878 1.00 18.70 1078 CG2 VAL A 476 20.197 76.685 14.934 1.00 20.99 1079 N GLN A 477 19.574 78.606 10.764 1.00 25.16 1080 CA GLN A 477 19.965 79.428 9.640 1.00 26.65 1081 C GLN A 477 19.263 80.767 9.662 1.00 26.62 1082 O GLN A 477 18.160 80.891 10.175 1.00 26.40 1083 CB GLN A 477 19.701 78.683 8.325 1.00 31.51 1084 CG GLN A 477 18.289 78.252 8.089 1.00 44.27 1085 CB GLN A 477 18.188 77.095 7.084 1.00 47.76 1086 OE1 GLN A 477 17.104 76.786 6.598 1.00 50.57 1087 NE2 GLN A 477 19.317 76.449 6.787 1.00 47.32 1088 N THR A 478 19.941 81.780 9.146 1.00 27.41 1089 CA THR A 478 19.375 83.112 9.074 1.00 28.36 1090 C THR A 478 18.944 83.408 7.635 1.00 30.10 1091 O THR A 478 19.567 82.940 6.672 1.00 25.31 1092 CB THR A 478 20.404 84.139 9.533 1.00 28.76 1093 CG THR A 478 20.649 84.098 11.013 1.00 34.11 1094 CD1 THR A 478 21.522 83.287 11.685 1.00 31.25 1095 CD2 THR A 478 19.980 84.878 12.006 1.00 31.01 1096 NE1 THR A 478 21.436 83.515 13.031 1.00 27.71 1097 CE2 THR A 478 20.496 84.487 13.259 1.00 31.95 1098 CE3 THR A 478 18.993 85.871 11.960 1.00 34.16 1099 CZ2 THR A 478 20.055 85.058 14.463 1.00 25.26 1100 CZ3 THR A 478 18.556 86.439 13.153 1.00 31.64 1101 CH2 THR A 478 19.089 86.029 14.387 1.00 28.89 1102 N LEU A 479 17.877 84.182 7.498 1.00 32.48 1103 CA LEU A 479 17.355 84.551 6.187 1.00 37.36 1104 C LEU A 479 16.943 86.016 6.140 1.00 40.42 1105 O LEU A 479 16.448 86.560 7.123 1.00 40.14 1106 CB LEU A 479 16.122 83.722 5.848 1.00 39.83 1107 CG LEU A 479 16.044 82.254 6.258 1.00 44.57 1108 CD1 LEU A 479 14.713 81.710 5.810 1.00 52.98 1109 CD2 LEU A 479 17.161 81.470 5.634 1.00 50.71 1110 N HIS A 480 17.152 86.653 4.998 1.00 43.05 1111 CA HIS A 480 16.723 88.028 4.824 1.00 49.20 1112 C HIS A 480 15.464 87.854 3.984 1.00 52.73 1113 O HIS A 480 15.509 87.895 2.753 1.00 52.90 1114 CB HIS A 480 17.756 88.846 4.057 1.00 52.25 1115 CG HIS A 480 17.330 90.259 3.814 1.00 57.22 1116 ND1 HIS A 480 17.525 91.263 4.736 1.00 61.37 1117 CD2 HIS A 480 16.658 90.822 2.781 1.00 59.16 1118 CE1 HIS A 480 16.993 92.384 4.285 1.00 59.88 1119 NE2 HIS A 480 16.460 92.144 3.100 1.00 66.11 1120 N ASN A 481 14.347 87.629 4.670 1.00 56.65 1121 CA ASN A 481 13.057 87.394 4.030 1.00 59.93 1122 C ASN A 481 13.009 85.940 3.581 1.00 59.65 1123 O ASN A 481 13.031 85.029 4.405 1.00 61.04 1124 CB ASN A 481 12.849 88.312 2.818 1.00 64.65 1125 CG ASN A 481 12.578 89.748 3.210 1.00 72.38 1126 OD1 ASN A 481 11.636 90.037 3.953 1.00 74.96 1127 ND2 ASN A 481 13.401 90.662 2.707 1.00 75.60 1128 N GLU A 482 12.975 85.728 2.273 1.00 58.97 1129 CA GLU A 482 12.903 84.387 1.704 1.00 58.55 1130 C GLU A 482 14.254 83.785 1.318 1.00 55.30 1131 O GLU A 482 14.347 82.587 1.056 1.00 57.27 1132 CB GLU A 482 11.993 84.424 0.473 1.00 65.42 1133 CG GLU A 482 11.787 85.840 −0.072 1.00 73.94 1134 CB GLU A 482 11.127 85.865 −1.432 1.00 80.29 1135 OE1 GLU A 482 11.770 85.432 −2.413 1.00 86.31 1136 OE2 GLU A 482 9.967 86.316 −1.520 1.00 82.73 1137 N VAL A 483 15.299 84.603 1.286 1.00 50.25 1138 CA VAL A 483 16.612 84.113 0.889 1.00 45.78 1139 C VAL A 483 17.575 83.867 2.048 1.00 43.04 1140 O VAL A 483 17.766 84.720 2.902 1.00 41.34 1141 CB VAL A 483 17.261 85.073 −0.133 1.00 43.76 1142 CG1 VAL A 483 17.317 86.471 0.432 1.00 46.25 1143 CG2 VAL A 483 18.654 84.589 −0.494 1.00 41.37 1144 N GLN A 484 18.188 82.688 2.050 1.00 42.30 1145 CA GLN A 484 19.126 82.300 3.095 1.00 43.21 1146 C GLN A 484 20.509 82.942 2.959 1.00 42.48 1147 O GLN A 484 21.055 83.062 1.856 1.00 41.64 1148 CB GLN A 484 19.269 80.774 3.129 1.00 45.96 1149 CG GLN A 484 20.331 80.276 4.101 1.00 54.43 1150 CD GLN A 484 20.427 78.760 4.159 1.00 59.02 1151 OE1 GLN A 484 21.400 78.209 4.677 1.00 59.71 1152 NE2 GLN A 484 19.410 78.078 3.636 1.00 61.46 1153 N LEU A 485 21.061 83.361 4.094 1.00 38.99 1154 CA LEU A 485 22.382 83.982 4.147 1.00 39.17 1155 C LEU A 485 23.458 82.900 4.247 1.00 40.35 1156 O LEU A 485 23.183 81.778 4.670 1.00 37.39 1157 CB LEU A 485 22.493 84.895 5.375 1.00 37.16 1158 CG LEU A 485 21.460 86.021 5.498 1.00 39.66 1159 CD1 LEU A 485 21.670 86.764 6.807 1.00 39.30 1160 CD2 LEU A 485 21.580 86.956 4.305 1.00 40.56 1161 N PRO A 486 24.700 83.227 3.858 1.00 42.55 1162 CA PRO A 486 25.772 82.234 3.942 1.00 46.30 1163 C PRO A 486 25.940 81.850 5.412 1.00 49.32 1164 O PRO A 486 25.748 82.684 6.294 1.00 48.81 1165 CB PRO A 486 26.991 82.994 3.425 1.00 45.64 1166 CG PRO A 486 26.413 84.068 2.572 1.00 45.29 1167 CD PRO A 486 25.206 84.505 3.331 1.00 40.65 1168 N ASP A 487 26.310 80.603 5.671 1.00 53.39 1169 CA ASP A 487 26.507 80.135 7.038 1.00 57.75 1170 C ASP A 487 27.603 80.940 7.750 1.00 57.25 1171 O ASP A 487 27.424 81.395 8.887 1.00 57.75 1172 CB ASP A 487 26.892 78.656 7.023 1.00 67.82 1173 CG ASP A 487 26.821 78.023 8.397 1.00 76.17 1174 OD1 ASP A 487 27.291 78.655 9.366 1.00 84.77 1175 OD2 ASP A 487 26.303 76.889 8.508 1.00 86.94 1176 N ALA A 488 28.727 81.122 7.065 1.00 54.64 1177 CA ALA A 488 29.871 81.848 7.607 1.00 53.45 1178 C ALA A 488 29.531 83.179 8.263 1.00 52.74 1179 O ALA A 488 30.359 83.757 8.966 1.00 53.06 1180 CB ALA A 488 30.892 82.070 6.515 1.00 53.75 1181 N ARG A 489 28.313 83.662 8.044 1.00 50.96 1182 CA ARG A 489 27.896 84.940 8.609 1.00 47.84 1183 C ARG A 489 27.436 84.895 10.064 1.00 45.10 1184 O ARG A 489 27.442 85.919 10.737 1.00 43.37 1185 CB ARG A 489 26.792 85.554 7.746 1.00 48.99 1186 CG ARG A 489 27.306 86.368 6.576 1.00 50.01 1187 CD ARG A 489 27.173 87.839 6.873 1.00 50.36 1188 NE ARG A 489 26.019 88.413 6.195 1.00 56.65 1189 CZ ARG A 489 25.434 89.552 6.543 1.00 58.23 1190 NH1 ARG A 489 25.886 90.248 7.578 1.00 61.07 1191 NH2 ARG A 489 24.407 90.006 5.840 1.00 59.63 1192 N HIS A 490 27.027 83.728 10.549 1.00 42.41 1193 CA HIS A 490 26.576 83.635 11.934 1.00 41.63 1194 C HIS A 490 27.390 82.648 12.766 1.00 39.71 1195 O HIS A 490 28.129 81.832 12.235 1.00 41.30 1196 CB HIS A 490 25.092 83.252 12.000 1.00 42.40 1197 CG HIS A 490 24.793 81.880 11.486 1.00 43.27 1198 ND1 HIS A 490 24.423 81.634 10.181 1.00 42.27 1199 CD2 HIS A 490 24.821 80.674 12.101 1.00 44.41 1200 CE1 HIS A 490 24.236 80.338 10.014 1.00 39.88 1201 NE2 HIS A 490 24.470 79.732 11.166 1.00 45.37 1202 N SER A 491 27.245 82.742 14.080 1.00 37.20 1203 CA SER A 491 27.946 81.866 15.005 1.00 36.36 1204 C SER A 491 26.915 81.199 15.927 1.00 33.06 1205 O SER A 491 26.172 81.879 16.639 1.00 33.77 1206 CB SER A 491 28.949 82.690 15.812 1.00 35.42 1207 OG SER A 491 29.547 81.906 16.818 1.00 43.65 1208 N THR A 492 26.878 79.872 15.912 1.00 29.90 1209 CA THR A 492 25.927 79.105 16.717 1.00 29.91 1210 C THR A 492 26.623 78.278 17.813 1.00 29.20 1211 O THR A 492 27.609 77.604 17.548 1.00 30.85 1212 CB THR A 492 25.094 78.153 15.802 1.00 29.85 1213 OG1 THR A 492 24.403 78.930 14.819 1.00 35.86 1214 CG2 THR A 492 24.059 77.366 16.602 1.00 28.05 1215 N THR A 493 26.095 78.319 19.035 1.00 29.49 1216 CA THR A 493 26.687 77.568 20.143 1.00 30.19 1217 C THR A 493 26.305 76.099 20.044 1.00 32.39 1218 O THR A 493 25.390 75.737 19.314 1.00 30.70 1219 CB THR A 493 26.222 78.098 21.532 1.00 27.82 1220 OG1 THR A 493 24.794 78.008 21.640 1.00 30.48 1221 CG2 THR A 493 26.647 79.533 21.728 1.00 22.03 1222 N GLN A 494 27.014 75.253 20.778 1.00 35.09 1223 CA GLN A 494 26.721 73.821 20.770 1.00 38.19 1224 C GLN A 494 25.509 73.568 21.651 1.00 36.48 1225 O GLN A 494 25.330 74.240 22.668 1.00 35.75 1226 CB GLN A 494 27.904 73.019 21.325 1.00 43.09 1227 CG GLN A 494 29.167 73.098 20.490 1.00 58.35 1228 CB GLN A 494 28.934 72.671 19.058 1.00 65.11 1229 OE1 GLN A 494 28.391 71.597 18.797 1.00 71.67 1230 NE2 GLN A 494 29.345 73.512 18.118 1.00 71.87 1231 N PRO A 495 24.661 72.598 21.272 1.00 36.89 1232 CA PRO A 495 23.470 72.278 22.063 1.00 38.37 1233 C PRO A 495 23.863 71.991 23.513 1.00 40.80 1234 O PRO A 495 24.837 71.286 23.773 1.00 40.76 1235 CB PRO A 495 22.920 71.043 21.371 1.00 37.83 1236 CG PRO A 495 23.300 71.285 19.926 1.00 40.41 1237 CD PRO A 495 24.716 71.791 20.039 1.00 35.81 1238 N ARG A 496 23.120 72.560 24.450 1.00 42.05 1239 CA ARG A 496 23.392 72.345 25.860 1.00 47.69 1240 C ARG A 496 22.146 71.828 26.558 1.00 51.66 1241 O ARG A 496 21.042 72.317 26.316 1.00 51.95 1242 CB ARG A 496 23.849 73.646 26.516 1.00 45.81 1243 CG ARG A 496 25.283 74.001 26.208 1.00 51.53 1244 CD ARG A 496 25.653 75.383 26.709 1.00 53.72 1245 NE ARG A 496 27.046 75.425 27.137 1.00 57.50 1246 CZ ARG A 496 27.478 74.992 28.317 1.00 58.59 1247 NH1 ARG A 496 26.626 74.489 29.199 1.00 57.22 1248 NH2 ARG A 496 28.768 75.058 28.612 1.00 65.31 1249 N LYS A 497 22.319 70.827 27.413 1.00 56.98 1250 CA LYS A 497 21.192 70.265 28.147 1.00 61.91 1251 C LYS A 497 20.733 71.299 29.145 1.00 63.97 1252 O LYS A 497 21.405 72.300 29.371 1.00 64.61 1253 CB LYS A 497 21.597 69.013 28.928 1.00 66.35 1254 CG LYS A 497 21.819 67.752 28.113 1.00 74.14 1255 CD LYS A 497 22.241 66.607 29.034 1.00 80.69 1256 CE LYS A 497 22.408 65.296 28.286 1.00 84.48 1257 NZ LYS A 497 22.861 64.215 29.211 1.00 88.26 1258 N THR A 498 19.583 71.045 29.748 1.00 67.67 1259 CA THR A 498 19.028 71.931 30.758 1.00 71.26 1260 C THR A 498 18.316 71.050 31.760 1.00 73.04 1261 O THR A 498 18.610 69.857 31.864 1.00 72.83 1262 CB THR A 498 18.015 72.921 30.155 1.00 71.80 1263 OG1 THR A 498 17.045 72.208 29.379 1.00 71.58 1264 CG2 THR A 498 18.722 73.930 29.281 1.00 73.61 1265 N LYS A 499 17.380 71.638 32.495 1.00 75.57 1266 CA LYS A 499 16.607 70.895 33.480 1.00 77.62 1267 C LYS A 499 15.458 70.173 32.779 1.00 77.92 1268 O LYS A 499 14.504 70.809 32.332 1.00 79.19 1269 CB LYS A 499 16.042 71.848 34.533 1.00 80.22 1270 CG LYS A 499 17.069 72.428 35.496 1.00 81.04 1271 CB LYS A 499 17.507 71.397 36.529 1.00 83.26 1272 CE LYS A 499 18.368 72.031 37.613 1.00 84.81 1273 NZ LYS A 499 18.736 71.055 38.675 1.00 86.04 1274 N GLY A 500 15.566 68.852 32.667 1.00 76.91 1275 CA GLY A 500 14.523 68.056 32.039 1.00 75.83 1276 C GLY A 500 14.040 68.459 30.655 1.00 75.14 1277 O GLY A 500 14.024 67.629 29.745 1.00 75.52 1278 N SER A 501 13.642 69.718 30.495 1.00 73.08 1279 CA SER A 501 13.132 70.230 29.225 1.00 71.65 1280 C SER A 501 13.764 69.592 27.994 1.00 68.64 1281 O SER A 501 13.085 68.910 27.223 1.00 71.13 1282 CB SER A 501 13.321 71.746 29.147 1.00 74.43 1283 OG SER A 501 14.667 72.076 28.859 1.00 80.92 1284 N GLY A 502 15.060 69.814 27.810 1.00 63.14 1285 CA GLY A 502 15.741 69.256 26.657 1.00 54.62 1286 C GLY A 502 16.982 70.048 26.297 1.00 48.04 1287 O GLY A 502 17.917 70.131 27.094 1.00 48.08 1288 N PHE A 503 17.001 70.642 25.106 1.00 40.50 1289 CA PHE A 503 18.173 71.411 24.692 1.00 33.81 1290 C PHE A 503 17.908 72.827 24.212 1.00 28.39 1291 O PHE A 503 16.789 73.192 23.856 1.00 26.35 1292 CB PHE A 503 18.938 70.681 23.583 1.00 35.09 1293 CG PHE A 503 19.452 69.337 23.981 1.00 34.16 1294 CD1 PHE A 503 18.630 68.219 23.926 1.00 35.05 1295 CD2 PHE A 503 20.755 69.189 24.430 1.00 35.90 1296 CE1 PHE A 503 19.099 66.967 24.317 1.00 36.00 1297 CE2 PHE A 503 21.238 67.944 24.826 1.00 40.04 1298 CZ PHE A 503 20.408 66.829 24.771 1.00 38.82 1299 N PHE A 504 18.967 73.625 24.216 1.00 26.16 1300 CA PHE A 504 18.891 74.988 23.731 1.00 25.00 1301 C PHE A 504 20.182 75.314 23.004 1.00 26.57 1302 O PHE A 504 21.221 74.708 23.267 1.00 26.73 1303 CB PHE A 504 18.640 75.984 24.858 1.00 22.46 1304 CG PHE A 504 19.834 76.270 25.718 1.00 27.70 1305 CD1 PHE A 504 20.674 77.340 25.433 1.00 28.94 1306 CD2 PHE A 504 20.083 75.514 26.857 1.00 31.34 1307 CE1 PHE A 504 21.743 77.662 26.273 1.00 30.08 1308 CE2 PHE A 504 21.151 75.828 27.704 1.00 32.65 1309 CZ PHE A 504 21.979 76.909 27.403 1.00 32.80 1310 N VAL A 505 20.091 76.270 22.085 1.00 23.68 1311 CA VAL A 505 21.211 76.705 21.286 1.00 24.67 1312 C VAL A 505 21.041 78.215 21.072 1.00 23.86 1313 O VAL A 505 19.928 78.725 21.049 1.00 21.24 1314 CB VAL A 505 21.208 75.926 19.939 1.00 27.95 1315 CG1 VAL A 505 20.134 76.464 19.020 1.00 25.61 1316 CG2 VAL A 505 22.558 75.957 19.314 1.00 33.51 1317 N PHE A 506 22.146 78.936 20.959 1.00 26.20 1318 CA PHE A 506 22.086 80.382 20.754 1.00 26.10 1319 C PHE A 506 22.846 80.745 19.479 1.00 24.83 1320 O PHE A 506 23.928 80.231 19.241 1.00 25.52 1321 CB PHE A 506 22.725 81.104 21.939 1.00 28.18 1322 CG PHE A 506 22.758 82.593 21.797 1.00 35.33 1323 CD1 PHE A 506 21.620 83.355 22.020 1.00 42.56 1324 CD2 PHE A 506 23.937 83.241 21.443 1.00 40.04 1325 CE1 PHE A 506 21.660 84.746 21.892 1.00 44.70 1326 CE2 PHE A 506 23.987 84.623 21.311 1.00 40.54 1327 CZ PHE A 506 22.851 85.377 21.536 1.00 42.12 1328 N SER A 507 22.290 81.639 18.673 1.00 24.69 1329 CA SER A 507 22.941 82.050 17.426 1.00 24.73 1330 C SER A 507 23.065 83.578 17.355 1.00 26.40 1331 O SER A 507 22.113 84.292 17.609 1.00 25.99 1332 CB SER A 507 22.151 81.521 16.221 1.00 22.19 1333 OG SER A 507 22.740 81.947 15.009 1.00 30.30 1334 N ARG A 508 24.255 84.062 17.009 1.00 26.98 1335 CA ARG A 508 24.545 85.496 16.913 1.00 25.95 1336 C ARG A 508 24.851 85.911 15.463 1.00 24.97 1337 O ARG A 508 25.621 85.250 14.785 1.00 24.35 1338 CB ARG A 508 25.755 85.801 17.790 1.00 21.97 1339 CG ARG A 508 26.249 87.235 17.756 1.00 25.32 1340 CD ARG A 508 27.474 87.372 18.656 1.00 25.67 1341 NE ARG A 508 27.898 88.758 18.788 1.00 36.00 1342 CZ ARG A 508 28.757 89.357 17.972 1.00 36.06 1343 NH1 ARG A 508 29.293 88.682 16.963 1.00 34.19 1344 NH2 ARG A 508 29.062 90.633 18.157 1.00 34.70 1345 N LEU A 509 24.269 87.017 15.001 1.00 26.44 1346 CA LEU A 509 24.492 87.479 13.621 1.00 28.45 1347 C LEU A 509 24.794 88.973 13.540 1.00 28.87 1348 O LEU A 509 23.893 89.797 13.699 1.00 30.99 1349 CB LEU A 509 23.259 87.177 12.758 1.00 27.28 1350 CG LEU A 509 23.270 87.733 11.321 1.00 31.90 1351 CD1 LEU A 509 24.284 86.985 10.453 1.00 29.48 1352 CD2 LEU A 509 21.886 87.599 10.732 1.00 28.89 1353 N GLU A 510 26.054 89.323 13.288 1.00 31.92 1354 CA GLU A 510 26.448 90.728 13.189 1.00 34.67 1355 C GLU A 510 26.005 91.290 11.845 1.00 36.35 1356 O GLU A 510 26.199 90.652 10.812 1.00 34.66 1357 CB GLU A 510 27.970 90.875 13.343 1.00 41.07 1358 CG GLU A 510 28.510 90.383 14.696 1.00 54.35 1359 CD GLU A 510 29.997 90.675 14.911 1.00 58.86 1360 OE1 GLU A 510 30.811 90.364 14.013 1.00 61.22 1361 OE2 GLU A 510 30.349 91.207 15.989 1.00 61.34 1362 N VAL A 511 25.406 92.479 11.852 1.00 36.50 1363 CA VAL A 511 24.935 93.069 10.606 1.00 38.05 1364 C VAL A 511 25.370 94.516 10.408 1.00 42.41 1365 O VAL A 511 25.744 95.205 11.368 1.00 41.92 1366 CB VAL A 511 23.403 93.012 10.508 1.00 31.84 1367 CG1 VAL A 511 22.927 91.585 10.669 1.00 32.42 1368 CG2 VAL A 511 22.787 93.913 11.553 1.00 26.87 1369 N THR A 512 25.310 94.967 9.154 1.00 43.58 1370 CA TNR A 512 25.697 96.331 8.808 1.00 48.37 1371 C THR A 512 24.602 97.306 9.201 1.00 50.53 1372 O THR A 512 23.487 96.894 9.516 1.00 51.77 1373 CB THR A 512 25.956 96.475 7.303 1.00 48.57 1374 OG1 THR A 512 24.766 96.140 6.581 1.00 46.96 1375 CG2 THR A 512 27.085 95.554 6.866 1.00 45.82 1376 N ARG A 513 24.922 98.598 9.188 1.00 53.29 1377 CA ARG A 513 23.952 99.629 9.544 1.00 55.54 1378 C ARG A 513 22.781 99.557 8.577 1.00 55.38 1379 O ARG A 513 21.623 99.741 8.962 1.00 55.22 1380 CB ARG A 513 24.594 101.018 9.464 1.00 59.23 1381 CG ARG A 513 23.999 102.037 10.428 1.00 65.98 1382 CD ARG A 513 22.519 102.274 10.184 1.00 74.12 1383 NE ARG A 513 21.858 102.827 11.365 1.00 80.97 1384 CZ ARG A 513 20.581 103.197 11.413 1.00 83.64 1385 NH1 ARG A 513 19.809 103.084 10.340 1.00 86.02 1386 NH2 ARG A 513 20.072 103.673 12.543 1.00 85.44 1387 N ALA A 514 23.099 99.285 7.317 1.00 55.03 1388 CA ALA A 514 22.096 99.186 6.268 1.00 55.46 1389 C ALA A 514 21.061 98.104 6.571 1.00 56.10 1390 O ALA A 514 19.866 98.390 6.674 1.00 56.61 1391 CB ALA A 514 22.775 98.908 4.927 1.00 54.05 1392 N GLU A 515 21.509 96.859 6.712 1.00 55.46 1393 CA GLU A 515 20.575 95.781 6.995 1.00 55.34 1394 C GLU A 515 19.949 95.951 8.371 1.00 54.83 1395 O GLU A 515 18.877 95.410 8.644 1.00 52.33 1396 CB GLU A 515 21.265 94.413 6.868 1.00 57.76 1397 CG GLU A 515 22.716 94.379 7.312 1.00 62.58 1398 CD GLU A 515 23.416 93.082 6.937 1.00 63.27 1399 OE1 GLU A 515 23.168 92.565 5.829 1.00 64.89 1400 OE2 GLU A 515 24.228 92.586 7.741 1.00 66.59 1401 N THR A 516 20.608 96.716 9.234 1.00 55.79 1402 CA THR A 516 20.072 96.956 10.566 1.00 57.81 1403 C THR A 516 18.818 97.822 10.464 1.00 58.51 1404 O THR A 516 17.988 97.822 11.374 1.00 57.71 1405 CB THR A 516 21.101 97.649 11.466 1.00 61.48 1406 CG THR A 516 20.738 97.544 12.913 1.00 66.54 1407 CD1 THR A 516 20.823 96.428 13.697 1.00 67.26 1408 CD2 THR A 516 20.140 98.561 13.725 1.00 69.56 1409 NE1 THR A 516 20.309 96.685 14.946 1.00 71.76 1410 CE2 THR A 516 19.882 97.987 14.990 1.00 70.88 1411 CE3 THR A 516 19.793 99.900 13.507 1.00 70.94 1412 CZ2 THR A 516 19.292 98.706 16.034 1.00 73.50 1413 CZ3 THR A 516 19.204 100.618 14.548 1.00 74.37 1414 CH2 THR A 516 18.961 100.016 15.796 1.00 74.71 1415 N GLU A 517 18.682 98.553 9.356 1.00 59.66 1416 CA GLU A 517 17.515 99.409 9.128 1.00 61.72 1417 C GLU A 517 16.301 98.565 8.746 1.00 59.87 1418 O GLU A 517 15.159 98.994 8.904 1.00 58.60 1419 CB GLU A 517 17.782 100.418 8.003 1.00 68.82 1420 CG GLU A 517 18.988 101.316 8.221 1.00 80.60 1421 CD GLU A 517 19.148 102.358 7.124 1.00 87.42 1422 OE1 GLU A 517 18.472 102.231 6.079 1.00 94.80 1423 OE2 GLU A 517 19.955 103.299 7.300 1.00 95.35 1424 N GLN A 518 16.555 97.366 8.233 1.00 57.92 1425 CA GLN A 518 15.480 96.468 7.836 1.00 55.74 1426 C GLN A 518 15.543 95.184 8.664 1.00 54.32 1427 O GLN A 518 15.207 94.102 8.176 1.00 52.85 1428 CB GLN A 518 15.600 96.146 6.355 1.00 54.10 1429 N LYS A 519 15.954 95.313 9.924 1.00 52.69 1430 CA LYS A 519 16.082 94.152 10.791 1.00 52.35 1431 C LYS A 519 14.781 93.394 10.941 1.00 51.69 1432 O LYS A 519 14.778 92.203 11.246 1.00 49.61 1433 CB LYS A 519 16.617 94.561 12.163 1.00 54.31 1434 CG LYS A 519 15.688 95.395 13.012 1.00 55.80 1435 CD LYS A 519 16.438 95.877 14.241 1.00 60.32 1436 CE LYS A 519 15.598 96.806 15.089 1.00 64.05 1437 NZ LYS A 519 16.409 97.377 16.202 1.00 70.92 1438 N ASP A 520 13.676 94.089 10.712 1.00 52.66 1439 CA ASP A 520 12.349 93.495 10.812 1.00 54.22 1440 C ASP A 520 12.204 92.391 9.764 1.00 53.07 1441 O ASP A 520 11.336 91.525 9.871 1.00 52.75 1442 CB ASP A 520 11.289 94.568 10.563 1.00 61.14 1443 CG ASP A 520 11.821 95.980 10.792 1.00 71.19 1444 OD1 ASP A 520 12.193 96.300 11.945 1.00 76.53 1445 OD2 ASP A 520 11.871 96.766 9.817 1.00 72.86 1446 N GLU A 521 13.067 92.423 8.757 1.00 51.01 1447 CA GLU A 521 13.018 91.443 7.684 1.00 50.49 1448 C GLU A 521 13.886 90.206 7.899 1.00 47.73 1449 O GLU A 521 13.762 89.228 7.165 1.00 48.58 1450 CB GLU A 521 13.400 92.107 6.362 1.00 53.54 1451 CG GLU A 521 12.423 93.173 5.901 1.00 60.11 1452 CD GLU A 521 12.901 93.895 4.658 1.00 65.41 1453 OE1 GLU A 521 13.103 93.239 3.614 1.00 67.98 1454 OE2 GLU A 521 13.079 95.129 4.726 1.00 73.58 1455 N PHE A 522 14.772 90.241 8.887 1.00 42.66 1456 CA PHE A 522 15.615 89.081 9.137 1.00 38.90 1457 C PHE A 522 14.847 88.017 9.892 1.00 35.93 1458 O PHE A 522 14.021 88.324 10.755 1.00 38.85 1459 CB PHE A 522 16.884 89.478 9.886 1.00 36.56 1460 CG PHE A 522 17.890 90.181 9.019 1.00 39.04 1461 CD1 PHE A 522 17.673 91.494 8.605 1.00 42.28 1462 CD2 PHE A 522 19.026 89.513 8.561 1.00 36.78 1463 CE1 PHE A 522 18.571 92.132 7.738 1.00 44.30 1464 CE2 PHE A 522 19.927 90.139 7.695 1.00 40.92 1465 CZ PHE A 522 19.699 91.454 7.283 1.00 39.51 1466 N ILE A 523 15.108 86.763 9.545 1.00 31.27 1467 CA ILE A 523 14.427 85.641 10.156 1.00 29.65 1468 C ILE A 523 15.389 84.551 10.617 1.00 29.13 1469 O ILE A 523 16.364 84.240 9.936 1.00 27.36 1470 CB ILE A 523 13.420 85.033 9.163 1.00 34.21 1471 CG1 ILE A 523 12.349 86.072 8.818 1.00 37.38 1472 CG2 ILE A 523 12.804 83.773 9.736 1.00 34.94 1473 CD1 ILE A 523 11.373 85.619 7.746 1.00 38.56 1474 N CYS A 524 15.102 83.990 11.789 1.00 26.34 1475 CA CYS A 524 15.901 82.914 12.361 1.00 27.10 1476 C CYS A 524 15.100 81.654 12.138 1.00 26.67 1477 O CYS A 524 13.945 81.590 12.531 1.00 27.58 1478 CB CYS A 524 16.103 83.127 13.874 1.00 24.27 1479 SG CYS A 524 16.974 81.777 14.737 1.00 37.60 1480 N ARG A 525 15.714 80.649 11.528 1.00 26.37 1481 CA ARG A 525 15.024 79.406 11.244 1.00 26.35 1482 C ARG A 525 15.713 78.181 11.796 1.00 26.72 1483 O ARG A 525 16.929 78.039 11.700 1.00 29.04 1484 CB ARG A 525 14.852 79.224 9.739 1.00 29.81 1485 CG ARG A 525 14.207 77.887 9.372 1.00 35.40 1486 CD ARG A 525 13.542 77.948 8.001 1.00 46.51 1487 NE ARG A 525 14.487 77.804 6.907 1.00 50.77 1488 CZ ARG A 525 14.221 78.139 5.649 1.00 55.09 1489 NH1 ARG A 525 13.035 78.649 5.337 1.00 54.58 1490 NH2 ARG A 525 15.136 77.950 4.703 1.00 56.77 1491 N ALA A 526 14.920 77.289 12.369 1.00 25.38 1492 CA ALA A 526 15.458 76.072 12.920 1.00 25.38 1493 C ALA A 526 14.872 74.879 12.175 1.00 25.99 1494 O ALA A 526 13.667 74.849 11.890 1.00 25.50 1495 CB ALA A 526 15.116 75.971 14.404 1.00 25.98 1496 N VAL A 527 15.728 73.916 11.841 1.00 23.84 1497 CA VAL A 527 15.267 72.705 11.198 1.00 25.15 1498 C VAL A 527 15.522 71.628 12.220 1.00 26.30 1499 O VAL A 527 16.642 71.481 12.706 1.00 26.20 1500 CB VAL A 527 16.043 72.365 9.923 1.00 24.43 1501 CG1 VAL A 527 15.610 71.012 9.439 1.00 26.95 1502 CG2 VAL A 527 15.781 73.409 8.849 1.00 28.13 1503 N HIS A 528 14.485 70.862 12.531 1.00 26.24 1504 CA HIS A 528 14.582 69.828 13.536 1.00 29.14 1505 C HIS A 528 13.498 68.778 13.295 1.00 31.86 1506 O HIS A 528 12.384 69.091 12.861 1.00 31.05 1507 CB HIS A 528 14.428 70.479 14.921 1.00 29.03 1508 CG HIS A 528 14.518 69.523 16.065 1.00 29.34 1509 ND1 HIS A 528 13.491 68.666 16.404 1.00 33.33 1510 CD2 HIS A 528 15.510 69.283 16.956 1.00 28.93 1511 CE1 HIS A 528 13.845 67.945 17.449 1.00 26.07 1512 NE2 HIS A 528 15.070 68.298 17.805 1.00 32.19 1513 N CLU A 529 13.843 67.536 13.599 1.00 34.08 1514 CA CLU A 529 12.964 66.393 13.424 1.00 39.76 1515 C CLU A 529 11.563 66.490 14.034 1.00 41.50 1516 O CLU A 529 10.580 66.190 13.360 1.00 41.48 1517 CB GLU A 529 13.641 65.138 13.978 1.00 43.03 1518 CG GLU A 529 12.702 63.935 14.014 1.00 56.19 1519 CD GLU A 529 13.239 62.773 14.826 1.00 62.66 1520 OE1 GLU A 529 12.489 61.788 15.007 1.00 63.52 1521 OE2 GLU A 529 14.402 62.842 15.281 1.00 65.43 1522 N ALA A 530 11.479 66.897 15.300 1.00 42.51 1523 CA ALA A 530 10.201 66.978 16.006 1.00 46.03 1524 C ALA A 530 9.269 68.105 15.596 1.00 49.29 1525 O ALA A 530 8.124 68.153 16.044 1.00 50.87 1526 CB ALA A 530 10.443 67.043 17.513 1.00 39.71 1527 N ALA A 531 9.751 69.005 14.748 1.00 52.89 1528 CA ALA A 531 8.949 70.133 14.302 1.00 56.14 1529 C ALA A 531 8.030 69.799 13.124 1.00 59.66 1530 O ALA A 531 8.258 70.243 12.004 1.00 61.00 1531 CB ALA A 531 9.864 71.295 13.938 1.00 52.83 1532 N SER A 532 6.992 69.012 13.370 1.00 63.07 1533 CA SER A 532 6.056 68.673 12.305 1.00 66.03 1534 C SER A 532 5.006 69.778 12.250 1.00 66.08 1535 O SER A 532 4.569 70.283 13.286 1.00 65.35 1536 CB SER A 532 5.384 67.330 12.593 1.00 68.98 1537 OG SER A 532 4.526 67.416 13.716 1.00 74.64 1538 N PRO A 533 4.581 70.173 11.043 1.00 66.51 1539 CA PRO A 533 4.931 69.713 9.696 1.00 65.99 1540 C PRO A 533 6.251 70.226 9.117 1.00 63.48 1541 O PRO A 533 6.760 71.273 9.518 1.00 64.33 1542 CB PRO A 533 3.757 70.203 8.873 1.00 69.06 1543 CG PRO A 533 3.539 71.556 9.471 1.00 71.08 1544 CB PRO A 533 3.570 71.242 10.963 1.00 70.23 1545 N SER A 534 6.783 69.466 8.165 1.00 59.21 1546 CA SER A 534 8.009 69.804 7.452 1.00 55.01 1547 C SER A 534 9.274 70.148 8.248 1.00 50.27 1548 O SER A 534 10.130 70.875 7.753 1.00 48.58 1549 CB SER A 534 7.706 70.934 6.475 1.00 58.20 1550 OG SER A 534 7.074 72.013 7.138 1.00 63.36 1551 N GLN A 535 9.387 69.616 9.461 1.00 44.89 1552 CA GLN A 535 10.543 69.829 10.330 1.00 42.88 1553 C GLN A 535 11.194 71.205 10.277 1.00 41.55 1554 O GLN A 535 12.419 71.321 10.294 1.00 40.80 1555 CB GLN A 535 11.633 68.769 10.080 1.00 37.08 1556 CG GLN A 535 11.302 67.731 9.056 1.00 47.40 1557 CD GLN A 535 10.101 66.916 9.431 1.00 44.36 1558 OE1 GLN A 535 9.193 66.738 8.625 1.00 47.59 1559 NE2 GLN A 535 10.079 66.415 10.664 1.00 54.70 1560 N THR A 536 10.387 72.252 10.226 1.00 39.97 1561 CA THR A 536 10.950 73.588 10.207 1.00 40.62 1562 C THR A 536 10.113 74.575 11.023 1.00 37.57 1563 O THR A 536 8.893 74.558 10.975 1.00 40.85 1564 CB THR A 536 11.137 74.092 8.747 1.00 42.38 1565 OG1 THR A 536 11.458 75.488 8.763 1.00 44.59 1566 CG2 THR A 536 9.881 73.870 7.932 1.00 49.65 1567 N VAL A 537 10.788 75.410 11.801 1.00 35.29 1568 CA VAL A 537 10.147 76.418 12.632 1.00 31.25 1569 C VAL A 537 10.996 77.678 12.537 1.00 29.01 1570 O VAL A 537 12.218 77.615 12.699 1.00 30.11 1571 CB VAL A 537 10.106 75.996 14.117 1.00 34.80 1572 CG1 VAL A 537 9.452 77.084 14.939 1.00 35.52 1573 CG2 VAL A 537 9.341 74.712 14.278 1.00 37.19 1574 N GLN A 538 10.365 78.820 12.292 1.00 26.73 1575 CA GLN A 538 11.107 80.067 12.167 1.00 26.74 1576 C GLN A 538 10.376 81.271 12.732 1.00 27.53 1577 O GLN A 538 9.169 81.249 12.902 1.00 29.89 1578 CB GLN A 538 11.424 80.335 10.700 1.00 28.48 1579 CG GLN A 538 10.208 80.624 9.834 1.00 25.88 1580 CD CLN A 538 10.595 80.853 8.378 1.00 28.51 1581 OE1 GLN A 538 11.390 80.102 7.810 1.00 31.66 1582 NE2 GLN A 538 10.035 81.885 7.772 1.00 27.39 1583 N ARG A 539 11.113 82.334 13.013 1.00 28.05 1584 CA ARG A 539 10.493 83.530 13.535 1.00 30.72 1585 C ARG A 539 11.288 84.742 13.114 1.00 31.33 1586 O ARG A 539 12.517 84.703 13.077 1.00 32.42 1587 CB ARG A 539 10.420 83.463 15.061 1.00 36.30 1588 CG ARG A 539 9.488 84.476 15.686 1.00 45.60 1589 CB ARG A 539 8.741 83.829 16.830 1.00 57.97 1590 NE ARG A 539 8.118 82.591 16.371 1.00 69.46 1591 CZ ARG A 539 7.453 81.745 17.150 1.00 78.18 1592 NH1 ARG A 539 7.316 81.996 18.447 1.00 83.01 1593 NH2 ARG A 539 6.927 80.641 16.630 1.00 81.89 1594 N ALA A 540 10.578 85.818 12.799 1.00 31.92 1595 CA ALA A 540 11.207 87.054 12.383 1.00 34.50 1596 C ALA A 540 11.691 87.774 13.634 1.00 36.68 1597 O ALA A 540 11.190 87.532 14.739 1.00 34.62 1598 CB ALA A 540 10.209 87.907 11.621 1.00 33.91 1599 N VAL A 541 12.694 88.626 13.460 1.00 39.73 1600 CA VAL A 541 13.254 89.386 14.572 1.00 44.47 1601 C VAL A 541 12.164 90.249 15.218 1.00 46.91 1602 O VAL A 541 11.595 91.124 14.573 1.00 44.53 1603 CB VAL A 541 14.415 90.295 14.090 1.00 42.49 1604 CG1 VAL A 541 14.715 91.358 15.130 1.00 47.96 1605 CG2 VAL A 541 15.655 89.460 13.831 1.00 42.43 1606 N SER A 542 11.869 89.997 16.489 1.00 52.25 1607 CA SER A 542 10.840 90.771 17.174 1.00 60.05 1608 C SER A 542 11.374 92.174 17.421 1.00 64.25 1609 O SER A 542 12.550 92.353 17.743 1.00 65.22 1610 CB SER A 542 10.443 90.110 18.500 1.00 60.43 1611 OG SER A 542 11.530 90.076 19.404 1.00 65.30 1612 N VAL A 543 10.510 93.168 17.256 1.00 68.19 1613 CA VAL A 543 10.906 94.557 17.444 1.00 72.45 1614 C VAL A 543 9.828 95.323 18.202 1.00 74.32 1615 O VAL A 543 8.970 95.979 17.603 1.00 75.99 1616 CB VAL A 543 11.148 95.247 16.084 1.00 74.41 1617 CG1 VAL A 543 11.530 96.705 16.299 1.00 76.37 1618 CG2 VAL A 543 12.233 94.514 15.318 1.00 75.78 1619 O HOH A 1 24.509 77.358 12.191 1.00 54.75 1620 O HOH A 2 7.537 85.444 12.546 1.00 37.27 1621 O HOH A 3 26.419 96.436 20.705 1.00 46.90 1622 O HOH A 4 27.452 65.238 9.563 1.00 44.93 1623 O HOH A 5 8.585 79.087 17.993 1.00 46.77 1624 O HOH A 6 22.224 80.929 7.089 1.00 40.32 1625 O HOH A 7 17.272 54.803 2.090 1.00 50.21 1626 O HOH A 8 30.340 75.004 30.685 1.00 61.75 1627 O HOH A 9 24.537 65.977 6.710 1.00 39.17 1628 O HOH A 10 16.841 94.781 2.897 1.00 64.36 1629 O HOH A 11 22.950 61.704 0.621 1.00 45.74 1630 O HOH A 12 28.469 65.195 7.094 1.00 39.34 1631 O HOH A 13 53.771 76.970 5.717 1.00 56.15 1632 O HOH A 14 28.128 87.403 13.055 1.00 46.48 1633 O HOH A 15 23.871 76.354 23.810 1.00 36.55 1634 O HOH A 16 28.656 78.595 14.195 1.00 48.95 1635 O HOH A 17 26.439 59.235 16.698 1.00 50.90 1636 O HOH A 18 48.822 76.573 10.696 1.00 58.83 1637 O HOH A 19 46.016 72.983 15.254 1.00 61.24 1638 O HOH A 20 18.011 59.153 0.608 1.00 58.37 1639 O HOH A 21 10.586 67.712 6.227 1.00 57.48 1640 O HOH A 22 39.217 50.176 20.140 1.00 60.62 1641 O HOH A 23 19.990 55.647 11.936 1.00 49.14 1642 O HOH A 24 18.092 104.938 6.774 1.00 63.67 1643 O HOH A 25 11.413 86.589 17.509 1.00 40.50 1644 O HOH A 26 55.940 62.358 0.863 1.00 58.12 1645 O HOH A 27 26.856 64.971 15.189 1.00 52.34 1646 O HOH A 28 32.914 64.797 12.453 1.00 52.41 1647 O HOH A 29 23.938 107.034 22.326 1.00 63.47 1648 O HOH A 30 28.142 76.042 14.972 1.00 56.91 1649 O HOH A 31 34.884 65.010 3.193 1.00 49.06 1650 O HOH A 32 10.166 82.530 4.732 1.00 59.31 1651 O HOH A 33 28.781 47.212 5.405 1.00 51.40 1652 O HOH A 34 26.373 54.646 2.184 1.00 49.71 1653 O HOH A 35 50.871 71.532 11.654 1.00 64.98 1654 O HOH A 36 14.970 75.672 2.416 1.00 55.97 1655 O HOH A 37 7.183 75.882 18.351 1.00 56.10 1656 O HOH A 38 8.889 71.461 23.144 1.00 48.69 1657 O HOH A 39 16.590 67.594 29.822 1.00 58.57 1658 O HOH A 40 38.458 52.685 18.905 1.00 54.81 1659 O HOH A 41 54.406 64.045 8.519 1.00 65.02 1660 O HOH A 42 10.751 53.102 5.496 1.00 60.95 1661 O HOH A 43 52.001 82.188 9.439 1.00 59.29 1662 O HOH A 44 16.985 77.359 2.354 1.00 64.70 1663 O HOH A 45 20.295 50.729 1.374 1.00 57.91 1664 O HOH A 46 23.952 95.782 3.814 1.00 54.20 1665 O HOH A 47 14.130 79.241 2.012 1.00 59.40 1666 O HOH A 48 42.373 77.528 8.231 1.00 61.07 1667 O HOH A 49 49.811 60.323 14.343 1.00 62.77 1668 O HOH A 50 32.587 60.842 17.597 1.00 54.90 1669 O HOH A 51 26.700 67.334 3.009 1.00 59.03 1670 O HOH A 52 27.137 97.388 12.542 1.00 57.55 1671 O HOH A 53 19.726 104.219 18.295 1.00 55.02 1672 O HOH A 54 27.571 78.794 11.807 1.00 62.62 1673 O HOH A 55 10.438 93.153 21.642 1.00 64.18 1674 O HOH A 56 20.189 101.789 21.921 1.00 57.80 1675 O HOH A 57 45.236 75.729 14.048 1.00 68.28 1676 O HOH A 58 28.726 86.130 15.755 1.00 42.77 1677 O HOH A 59 15.761 61.916 22.864 1.00 49.12 1678 O HOH A 60 18.673 97.101 18.412 1.00 60.00 1679 O HOH A 61 51.586 62.841 8.977 1.00 66.82 1680 O HOH A 62 12.665 48.318 9.830 1.00 61.58 1681 O HOH A 63 10.994 69.841 26.147 1.00 54.56 1682 O HOH A 64 34.004 50.096 9.090 1.00 52.20 1683 O HOH A 65 22.928 54.076 3.637 1.00 63.55 1684 O HOH A 66 13.124 80.438 22.463 1.00 49.41 1685 O HOH A 67 14.496 84.734 3.782 1.00 59.74 1686 O HOH A 68 33.203 84.033 9.037 1.00 61.59 1687 O HOH A 69 25.151 70.683 28.546 1.00 58.32 1688 O HOH A 70 43.528 47.541 7.082 1.00 67.46 1689 O HOH A 71 28.976 58.922 3.873 1.00 56.29 1690 O HOH A 72 39.085 57.630 3.442 1.00 57.89 1691 O HOH A 73 34.708 46.624 11.157 1.00 61.84 1692 O HOH A 74 3.300 67.675 10.833 1.00 70.53 1693 O HOH A 75 23.591 70.505 16.477 1.00 53.22 1694 O HOH A 76 15.993 56.650 1.105 1.00 60.73 1695 O HOH A 77 51.586 54.551 5.644 1.00 64.35 1696 O HOH A 78 14.626 95.986 18.718 1.00 59.27 1697 O HOH A 79 23.734 74.708 12.176 1.00 53.70 1698 O HOH A 80 17.100 96.977 3.795 1.00 60.32 1699 O HOH A 81 9.533 67.755 26.736 1.00 56.40 1700 O HOH A 82 18.888 66.846 28.479 1.00 62.11 1701 O HOH A 83 43.839 71.746 16.116 1.00 57.66 1702 O HOH A 84 8.517 74.508 22.311 1.00 61.70 1703 O HOH A 85 41.870 49.996 21.891 1.00 61.38 1704 O HOH A 86 14.562 94.919 2.718 1.00 67.86 1705 O HOH A 87 28.791 96.969 19.836 1.00 61.99 1706 O HOH A 88 23.437 78.234 7.551 1.00 54.45 1707 O HOH A 89 29.614 80.314 4.323 1.00 57.86 1708 O HOH A 90 28.546 67.893 5.438 1.00 58.43 1709 O HOH A 91 47.040 72.908 13.045 1.00 67.78 1710 O HOH A 92 42.407 51.656 18.123 1.00 65.22 1711 O HOH A 93 23.749 65.735 −2.072 1.00 60.31 1712 O HOH A 94 44.018 74.292 16.194 1.00 61.54 1713 O HOH A 95 11.601 46.086 10.312 1.00 67.64 1714 O HOH A 96 6.175 66.153 17.508 1.00 56.59 1715 O HOH A 97 31.504 47.151 3.997 1.00 64.62 1716 O HOH A 98 42.312 75.926 6.322 1.00 66.03 1717 O HOH A 99 31.022 57.142 18.155 1.00 62.65 1718 O HOH A 100 17.995 104.383 3.752 1.00 63.95 1719 O HOH A 101 10.716 86.701 −4.491 1.00 63.86 1720 O HOH A 102 27.763 72.631 16.379 1.00 62.58 1721 O HOH A 103 15.381 105.037 7.270 1.00 58.40 1722 O HOH A 104 47.651 78.799 15.518 1.00 61.34 1723 O HOH A 105 34.927 94.559 9.949 1.00 65.87 1724 O HOH A 106 9.087 82.761 20.779 1.00 61.27 1725 O HOH A 107 22.682 53.866 0.739 1.00 67.17 1726 O HOH A 108 37.349 58.563 −1.263 1.00 54.90 1727 O HOH A 109 24.982 97.874 2.783 1.00 66.23 1728 O HOH A 110 31.881 73.012 28.973 1.00 59.96 1729 O HOH A 111 47.953 60.989 1.790 1.00 64.92 1730 O HOH A 112 42.129 73.312 10.101 1.00 65.68 1731 O HOH A 113 36.875 58.541 1.642 1.00 61.47 1732 O HOH A 114 35.326 52.952 2.865 1.00 60.20 1733 O HOH A 115 6.136 77.374 20.212 1.00 59.29 1734 O HOH A 116 25.741 94.929 18.879 1.00 53.05 1735 O HOH A 117 54.362 58.376 9.533 1.00 69.15 1736 O HOH A 118 23.326 103.523 17.163 1.00 62.28 1737 O HOH A 119 5.978 83.975 15.596 1.00 59.61 1738 O HOH A 120 33.072 54.315 0.721 1.00 61.94 1739 O HOH A 121 37.197 45.372 11.843 1.00 64.45 1740 O HOH A 122 11.834 65.339 3.962 1.00 63.01 1741 O HOH A 123 16.132 79.865 0.613 1.00 59.29 1742 O HOH A 124 12.804 74.215 0.796 1.00 61.69 1743 O HOH A 125 6.166 72.199 12.094 1.00 69.10 1744 O HOH A 126 46.672 51.916 3.111 1.00 61.79 1745 O HOH A 127 21.940 56.684 −1.243 1.00 63.74 1746 O HOH A 128 19.803 72.626 40.522 1.00 67.04 1747 O HOH A 129 28.002 103.109 11.797 1.00 62.20 1748 O HOH A 130 16.264 66.529 27.554 1.00 66.48 1749 O HOH A 131 38.684 71.694 5.498 1.00 70.79 1750 O HOH A 132 30.875 98.591 19.410 1.00 72.41 1751 O HOH A 133 20.444 64.387 22.091 1.00 62.09 1752 O HOH A 134 16.959 52.193 1.564 1.00 61.32 1753 O HOH A 135 43.707 44.495 7.969 1.00 68.49 1754 O HOH A 136 27.297 51.198 3.047 1.00 69.04 1755 O HOH A 137 45.002 47.522 9.091 1.00 63.49 1756 O HOH A 138 20.670 82.001 0.631 1.00 53.37 1757 O HOH A 139 18.747 100.351 20.086 1.00 59.07 1758 O HOH A 140 43.001 46.804 15.782 1.00 65.35 1759 O HOH A 141 56.594 54.897 10.204 1.00 67.74 1760 O HOH A 142 16.980 94.578 0.460 1.00 67.40 1761 O HOH A 143 34.493 68.011 5.655 1.00 64.43 1762 O HOH A 144 7.561 88.413 1.394 1.00 67.27 1763 O HOH A 145 55.370 75.436 6.692 1.00 70.07 1764 N VAL B 336 42.982 59.443 29.109 1.00 58.93 1765 CA VAL B 336 43.788 60.200 30.107 1.00 60.44 1766 C VAL B 336 44.173 61.587 29.599 1.00 60.07 1767 O VAL B 336 45.211 61.753 28.958 1.00 61.48 1768 CB VAL B 336 45.079 59.445 30.453 1.00 60.81 1769 CG1 VAL B 336 45.794 60.136 31.600 1.00 61.71 1770 CG2 VAL B 336 44.755 58.010 30.798 1.00 64.73 1771 N SER B 337 43.343 62.583 29.891 1.00 57.95 1772 CA SER B 337 43.617 63.945 29.452 1.00 56.60 1773 C SER B 337 43.758 64.917 30.624 1.00 55.17 1774 O SER B 337 43.338 64.619 31.748 1.00 54.55 1775 CB SER B 337 42.522 64.415 28.497 1.00 57.92 1776 OG SER B 337 41.244 64.111 29.013 1.00 64.70 1777 N ALA B 338 44.362 66.073 30.357 1.00 52.40 1778 CA ALA B 338 44.590 67.078 31.389 1.00 50.69 1779 C ALA B 338 44.300 68.491 30.908 1.00 50.25 1780 O ALA B 338 44.538 68.828 29.746 1.00 51.17 1781 CB ALA B 338 46.027 66.989 31.889 1.00 50.21 1782 N TYR B 339 43.792 69.319 31.816 1.00 48.22 1783 CA TYR B 339 43.461 70.701 31.495 1.00 46.82 1784 C TYR B 339 43.834 71.610 32.669 1.00 44.51 1785 O TYR B 339 43.711 71.228 33.832 1.00 42.27 1786 CB TYR B 339 41.962 70.835 31.185 1.00 50.52 1787 CG TYR B 339 41.402 69.731 30.307 1.00 58.40 1788 CD1 TYR B 339 41.155 68.456 30.826 1.00 61.23 1789 CD2 TYR B 339 41.144 69.952 28.949 1.00 60.99 1790 CE1 TYR B 339 40.671 67.426 30.019 1.00 62.71 1791 CE2 TYR B 339 40.657 68.926 28.131 1.00 63.53 1792 CZ TYR B 339 40.424 67.667 28.673 1.00 64.33 1793 OH TYR B 339 39.956 66.647 27.870 1.00 65.07 1794 N LEU B 340 44.309 72.807 32.354 1.00 41.90 1795 CA LEU B 340 44.695 73.769 33.372 1.00 41.06 1796 C LEU B 340 43.929 75.029 33.022 1.00 41.10 1797 O LEU B 340 43.953 75.464 31.876 1.00 43.45 1798 CB LEU B 340 46.208 74.017 33.321 1.00 36.93 1799 CG LEU B 340 46.830 74.911 34.399 1.00 35.91 1800 CD1 LEU B 340 46.500 74.371 35.786 1.00 34.60 1801 CD2 LEU B 340 48.336 74.979 34.194 1.00 35.51 1802 N SER B 341 43.232 75.610 33.992 1.00 39.82 1803 CA SER B 341 42.448 76.810 33.715 1.00 39.85 1804 C SER B 341 42.955 78.002 34.486 1.00 37.88 1805 O SER B 341 43.524 77.863 35.556 1.00 42.10 1806 CB SER B 341 40.973 76.575 34.058 1.00 39.34 1807 OG SER B 341 40.808 76.253 35.428 1.00 44.58 1808 N ARG B 342 42.732 79.185 33.942 1.00 36.98 1809 CA ARG B 342 43.163 80.413 34.583 1.00 35.20 1810 C ARG B 342 42.183 80.747 35.707 1.00 33.18 1811 O ARG B 342 41.157 80.092 35.848 1.00 33.16 1812 CB ARG B 342 43.206 81.530 33.534 1.00 38.57 1813 CG ARG B 342 44.219 81.279 32.411 1.00 39.10 1814 CD ARG B 342 44.236 82.409 31.388 1.00 43.21 1815 NE ARG B 342 43.056 82.369 30.530 1.00 45.40 1816 CZ ARG B 342 42.886 81.514 29.527 1.00 48.22 1817 NH1 ARG B 342 43.823 80.623 29.240 1.00 52.78 1818 NH2 ARG B 342 41.769 81.541 28.814 1.00 54.34 1819 N PRO B 343 42.488 81.757 36.530 1.00 33.03 1820 CA PRO B 343 41.560 82.103 37.619 1.00 34.14 1821 C PRO B 343 40.261 82.693 37.065 1.00 34.06 1822 O PRO B 343 40.259 83.298 35.994 1.00 35.44 1823 CB PRO B 343 42.334 83.152 38.433 1.00 33.07 1824 CG PRO B 343 43.789 82.900 38.075 1.00 35.06 1825 CD PRO B 343 43.715 82.571 36.601 1.00 33.27 1826 N SER B 344 39.155 82.520 37.775 1.00 32.17 1827 CA SER B 344 37.909 83.110 37.308 1.00 31.75 1828 C SER B 344 37.983 84.586 37.686 1.00 32.07 1829 O SER B 344 38.485 84.940 38.756 1.00 30.21 1830 CB SER B 344 36.693 82.456 37.982 1.00 32.20 1831 OG SER B 344 36.487 82.935 39.301 1.00 32.50 1832 N PRO B 345 37.512 85.473 36.800 1.00 32.31 1833 CA PRO B 345 37.561 86.899 37.125 1.00 30.84 1834 C PRO B 345 36.890 87.219 38.471 1.00 29.64 1835 O PRO B 345 37.344 88.094 39.209 1.00 30.14 1836 CB PRO B 345 36.859 87.545 35.926 1.00 30.96 1837 CG PRO B 345 37.299 86.659 34.793 1.00 33.18 1838 CD PRO B 345 37.143 85.261 35.387 1.00 33.65 1839 N PHE B 346 35.831 86.497 38.808 1.00 28.34 1840 CA PHE B 346 35.153 86.756 40.066 1.00 31.46 1841 C PHE B 346 36.078 86.515 41.269 1.00 32.46 1842 O PHE B 346 36.135 87.331 42.193 1.00 32.59 1843 CB PHE B 346 33.894 85.889 40.184 1.00 32.72 1844 CG PHE B 346 33.218 85.987 41.521 1.00 36.34 1845 CD1 PHE B 346 32.619 87.170 41.928 1.00 40.58 1846 CD2 PHE B 346 33.189 84.898 42.378 1.00 36.76 1847 CE1 PHE B 346 31.991 87.267 43.167 1.00 38.98 1848 CE2 PHE B 346 32.563 84.985 43.618 1.00 40.15 1849 CZ PHE B 346 31.963 86.175 44.014 1.00 38.60 1850 N ASP B 347 36.803 85.397 41.250 1.00 32.92 1851 CA ASP B 347 37.723 85.066 42.336 1.00 33.58 1852 C ASP B 347 38.896 86.045 42.367 1.00 34.26 1853 O ASP B 347 39.388 86.408 43.434 1.00 32.29 1854 CB ASP B 347 38.251 83.633 42.179 1.00 28.72 1855 CG ASP B 347 37.236 82.592 42.579 1.00 39.62 1856 OD1 ASP B 347 37.515 81.375 42.429 1.00 42.08 1857 OD2 ASP B 347 36.151 82.991 43.054 1.00 46.23 1858 N LEU B 348 39.324 86.480 41.189 1.00 34.31 1859 CA LEU B 348 40.441 87.403 41.064 1.00 37.70 1860 C LEU B 348 40.159 88.858 41.471 1.00 38.98 1861 O LEU B 348 40.949 89.463 42.198 1.00 38.11 1862 CB LEU B 348 40.959 87.380 39.618 1.00 40.66 1863 CG LEU B 348 42.159 88.267 39.260 1.00 41.99 1864 CD1 LEU B 348 43.388 87.862 40.095 1.00 42.77 1865 CD2 LEU B 348 42.469 88.124 37.759 1.00 41.00 1866 N PHE B 349 39.040 89.417 41.017 1.00 39.68 1867 CA PHE B 349 38.725 90.819 41.306 1.00 42.09 1868 C PHE B 349 37.717 91.134 42.405 1.00 45.09 1869 O PHE B 349 37.821 92.169 43.062 1.00 48.27 1870 CB PHE B 349 38.272 91.526 40.029 1.00 37.36 1871 CG PHE B 349 39.244 91.411 38.900 1.00 36.93 1872 CD1 PHE B 349 38.976 90.579 37.818 1.00 38.16 1873 CD2 PHE B 349 40.444 92.113 38.926 1.00 38.04 1874 CE1 PHE B 349 39.885 90.445 36.781 1.00 38.11 1875 CE2 PHE B 349 41.369 91.986 37.887 1.00 37.58 1876 CZ PHE B 349 41.089 91.151 36.817 1.00 40.39 1877 N ILE B 350 36.726 90.277 42.600 1.00 46.66 1878 CA ILE B 350 35.746 90.548 43.639 1.00 48.94 1879 C ILE B 350 36.200 89.905 44.950 1.00 51.15 1880 O ILE B 350 36.505 90.593 45.921 1.00 50.51 1881 CB ILE B 350 34.359 90.008 43.240 1.00 48.52 1882 CG1 ThE B 350 34.038 90.428 41.801 1.00 49.25 1883 CG2 ILE B 350 33.300 90.548 44.177 1.00 49.68 1884 CD1 ILE B 350 34.242 91.911 41.533 1.00 46.80 1885 N ARG B 351 36.265 88.579 44.945 1.00 52.64 1886 CA ARG B 351 36.669 87.793 46.100 1.00 53.76 1887 C ARG B 351 38.114 88.090 46.519 1.00 53.61 1888 O ARG B 351 38.436 88.094 47.703 1.00 53.55 1889 CB ARG B 351 36.505 86.313 45.759 1.00 56.64 1890 CG ARG B 351 36.016 85.434 46.894 1.00 62.18 1891 CD ARG B 351 35.073 84.375 46.348 1.00 66.96 1892 NE ARG B 351 34.958 83.211 47.219 1.00 71.13 1893 CZ ARG B 351 35.957 82.371 47.470 1.00 76.72 1894 NH1 ARG B 351 37.145 82.573 46.916 1.00 78.73 1895 NH2 ARG B 351 35.771 81.325 48.268 1.00 77.63 1896 N LYS B 352 38.974 88.347 45.540 1.00 53.86 1897 CA LYS B 352 40.385 88.646 45.788 1.00 54.12 1898 C LYS B 352 41.172 87.449 46.328 1.00 52.02 1899 O LYS B 352 42.078 87.604 47.146 1.00 51.77 1900 CB LYS B 352 40.525 89.825 46.753 1.00 57.77 1901 CG LYS B 352 39.911 91.124 46.254 1.00 62.15 1902 CB LYS B 352 40.161 92.252 47.254 1.00 71.06 1903 CE LYS B 352 39.351 93.502 46.929 1.00 74.25 1904 NZ LYS B 352 37.893 93.307 47.185 1.00 78.35 1905 N SER B 353 40.811 86.258 45.867 1.00 48.01 1906 CA SER B 353 41.488 85.032 46.268 1.00 45.29 1907 C SER B 353 41.446 84.056 45.084 1.00 40.67 1908 O SER B 353 40.725 83.054 45.106 1.00 40.76 1909 CB SER B 353 40.809 84.423 47.498 1.00 47.97 1910 OG SER B 353 39.445 84.152 47.247 1.00 56.20 1911 N PRO B 354 42.225 84.356 44.030 1.00 36.53 1912 CA PRO B 354 42.361 83.596 42.781 1.00 32.68 1913 C PRO B 354 42.940 82.201 42.961 1.00 31.88 1914 O PRO B 354 43.813 81.985 43.798 1.00 29.76 1915 CB PRO B 354 43.306 84.453 41.940 1.00 30.29 1916 CG PRO B 354 43.260 85.801 42.587 1.00 41.68 1917 CD PRO B 354 43.155 85.494 44.035 1.00 33.29 1918 N THR B 355 42.446 81.258 42.168 1.00 30.03 1919 CA THR B 355 42.956 79.896 42.198 1.00 29.70 1920 C THR B 355 43.022 79.364 40.774 1.00 30.82 1921 O THR B 355 42.302 79.827 39.887 1.00 30.67 1922 CB THR B 355 42.042 78.931 42.964 1.00 32.14 1923 OG1 THR B 355 40.815 78.794 42.240 1.00 29.97 1924 CG2 THR B 355 41.763 79.425 44.393 1.00 31.76 1925 N ILE B 356 43.907 78.405 40.542 1.00 30.53 1926 CA ILE B 356 43.969 77.784 39.232 1.00 31.56 1927 C ILE B 356 43.740 76.321 39.525 1.00 31.79 1928 O ILE B 356 44.039 75.848 40.625 1.00 30.35 1929 CB ILE B 356 45.315 78.016 38.517 1.00 30.05 1930 CG1 ILE B 356 46.467 77.499 39.371 1.00 31.32 1931 CG2 ILE B 356 45.469 79.508 38.210 1.00 31.27 1932 CD1 ILE B 356 47.828 77.757 38.763 1.00 36.89 1933 N THR B 357 43.198 75.605 38.550 1.00 33.31 1934 CA THR B 357 42.881 74.205 38.751 1.00 33.68 1935 C THR B 357 43.403 73.318 37.644 1.00 35.47 1936 O THR B 357 43.228 73.607 36.459 1.00 36.65 1937 CB THR B 357 41.335 74.011 38.855 1.00 33.81 1938 OG1 THR B 357 40.844 74.683 40.023 1.00 33.71 1939 CG2 THR B 357 40.968 72.535 38.921 1.00 29.63 1940 N CYS B 358 44.034 72.228 38.048 1.00 35.41 1941 CA CYS B 358 44.561 71.254 37.110 1.00 38.12 1942 C CYS B 358 43.570 70.093 37.165 1.00 37.77 1943 O CYS B 358 43.395 69.473 38.210 1.00 36.67 1944 CB CYS B 358 45.945 70.789 37.568 1.00 40.37 1945 SG CYS B 358 46.871 69.769 36.374 1.00 49.83 1946 N LEU B 359 42.909 69.822 36.046 1.00 39.77 1947 CA LEU B 359 41.932 68.747 35.973 1.00 42.86 1948 C LEU B 359 42.432 67.593 35.123 1.00 46.01 1949 O LEU B 359 42.748 67.769 33.948 1.00 47.43 1950 CB LEU B 359 40.612 69.265 35.389 1.00 42.74 1951 CG LEU B 359 39.604 68.208 34.904 1.00 45.03 1952 CB1 LEU B 359 39.152 67.338 36.057 1.00 47.59 1953 CD2 LEU B 359 38.403 68.889 34.262 1.00 47.51 1954 N VAL B 360 42.493 66.411 35.721 1.00 48.26 1955 CA VAL B 360 42.931 65.220 35.010 1.00 52.34 1956 C VAL B 360 41.765 64.243 34.883 1.00 55.48 1957 O VAL B 360 41.092 63.928 35.866 1.00 55.57 1958 CB VAL B 360 44.100 64.527 35.747 1.00 53.36 1959 CG1 VAL B 360 44.481 63.240 35.029 1.00 51.62 1960 CG2 VAL B 360 45.299 65.467 35.816 1.00 51.77 1961 N VAL B 361 41.520 63.773 33.665 1.00 58.92 1962 CA VAL B 361 40.433 62.834 33.416 1.00 63.13 1963 C VAL B 361 40.993 61.506 32.926 1.00 67.77 1964 O VAL B 361 41.738 61.466 31.946 1.00 68.38 1965 CB VAL B 361 39.442 63.377 32.353 1.00 60.50 1966 CG1 VAL B 361 38.358 62.355 32.086 1.00 56.92 1967 CG2 VAL B 361 38.814 64.671 32.830 1.00 56.10 1968 N ASP B 362 40.635 60.426 33.615 1.00 72.90 1969 CA ASP B 362 41.098 59.085 33.259 1.00 78.30 1970 C ASP B 362 39.904 58.244 32.816 1.00 81.68 1971 O ASP B 362 39.168 57.709 33.648 1.00 81.72 1972 CB ASP B 362 41.771 58.415 34.462 1.00 80.22 1973 CG ASP B 362 42.530 57.156 34.080 1.00 84.67 1974 OD1 ASP B 362 42.113 56.478 33.117 1.00 87.54 1975 OD2 ASP B 362 43.537 56.837 34.749 1.00 87.19 1976 N LEU B 363 39.723 58.126 31.503 1.00 85.84 1977 CA LEU B 363 38.614 57.366 30.935 1.00 89.95 1978 C LEU B 363 38.562 55.923 31.428 1.00 92.20 1979 O LEU B 363 37.483 55.386 31.668 1.00 92.55 1980 CB LEU B 363 38.694 57.390 29.409 1.00 91.66 1981 CG LEU B 363 38.719 58.777 28.758 1.00 92.93 1982 CB1 LEU B 363 38.813 58.624 27.246 1.00 95.41 1983 CD2 LEU B 363 37.471 59.551 29.137 1.00 92.73 1984 N ALA B 364 39.726 55.296 31.573 1.00 94.76 1985 CA ALA B 364 39.801 53.916 32.051 1.00 97.66 1986 C ALA B 364 40.794 53.831 33.210 1.00 99.72 1987 O ALA B 364 41.998 53.996 33.021 1.00 100.44 1988 CB ALA B 364 40.235 52.996 30.921 1.00 97.99 1989 N PRO B 365 40.297 53.577 34.429 1.00 101.15 1990 CA PRO B 365 41.173 53.484 35.602 1.00 102.25 1991 C PRO B 365 41.895 52.163 35.855 1.00 103.43 1992 O PRO B 365 41.274 51.103 35.934 1.00 104.19 1993 CB PRO B 365 40.237 53.829 36.761 1.00 101.91 1994 CG PRO B 365 39.121 54.617 36.098 1.00 102.27 1995 CB PRO B 365 38.910 53.833 34.846 1.00 101.40 1996 N SER B 366 43.215 52.256 35.979 1.00 104.18 1997 CA SER B 366 44.088 51.132 36.299 1.00 104.43 1998 C SER B 366 44.573 51.676 37.637 1.00 104.05 1999 O SER B 366 44.888 52.864 37.727 1.00 104.36 2000 CB SER B 366 45.249 51.055 35.312 1.00 105.50 2001 OG SER B 366 46.040 52.223 35.413 1.00 106.70 2002 N LYS B 367 44.645 50.861 38.682 1.00 103.19 2003 CA LYS B 367 45.041 51.462 39.944 1.00 102.08 2004 C LYS B 367 46.491 51.630 40.367 1.00 100.74 2005 O LYS B 367 47.234 50.683 40.640 1.00 101.05 2006 CB LYS B 367 44.236 50.868 41.102 1.00 103.30 2007 CG LYS B 367 44.343 49.384 41.345 1.00 105.00 2008 CD LYS B 367 43.374 49.046 42.467 1.00 104.80 2009 CE LYS B 367 43.467 47.610 42.930 1.00 104.70 2010 NZ LYS B 367 42.524 47.386 44.066 1.00 105.18 2011 N GLY B 368 46.839 52.909 40.422 1.00 98.70 2012 CA GLY B 368 48.136 53.408 40.828 1.00 95.62 2013 C GLY B 368 47.700 54.801 41.244 1.00 93.12 2014 O GLY B 368 46.538 55.143 41.035 1.00 93.17 2015 N THR B 369 48.569 55.617 41.823 1.00 90.15 2016 CA THR B 369 48.125 56.948 42.220 1.00 86.41 2017 C THR B 369 48.420 57.977 41.136 1.00 83.04 2018 O THR B 369 49.402 57.854 40.401 1.00 82.54 2019 CB THR B 369 48.792 57.397 43.541 1.00 87.73 2020 OG1 THR B 369 50.217 57.422 43.379 1.00 88.60 2021 CG2 THR B 369 48.423 56.443 44.671 1.00 86.64 2022 N VAL B 370 47.552 58.980 41.027 1.00 79.07 2023 CA VAL B 370 47.729 60.041 40.042 1.00 74.46 2024 C VAL B 370 48.275 61.261 40.768 1.00 72.21 2025 O VAL B 370 47.602 61.838 41.618 1.00 71.35 2026 CB VAL B 370 46.401 60.420 39.368 1.00 73.33 2027 CG1 VAL B 370 46.667 61.346 38.196 1.00 70.92 2028 CG2 VAL B 370 45.674 59.173 38.915 1.00 69.77 2029 N ASN B 371 49.498 61.653 40.426 1.00 70.13 2030 CA ASN B 371 50.137 62.791 41.073 1.00 68.15 2031 C ASN B 371 50.157 64.079 40.262 1.00 65.65 2032 O ASN B 371 50.352 64.067 39.046 1.00 64.64 2033 CB ASN B 371 51.564 62.421 41.469 1.00 70.12 2034 CG ASN B 371 51.605 61.330 42.508 1.00 73.56 2035 OD1 ASN B 371 51.153 61.519 43.638 1.00 75.10 2036 ND2 ASN B 371 52.137 60.173 42.131 1.00 74.76 2037 N LEU B 372 49.949 65.192 40.959 1.00 62.66 2038 CA LEU B 372 49.959 66.512 40.346 1.00 59.53 2039 C LEU B 372 50.927 67.374 41.137 1.00 56.68 2040 O LEU B 372 50.788 67.529 42.347 1.00 56.70 2041 CB LEU B 372 48.560 67.141 40.372 1.00 59.44 2042 CG LEU B 372 47.428 66.383 39.678 1.00 60.55 2043 CD1 LEU B 372 46.214 67.277 39.579 1.00 61.28 2044 CD2 LEU B 372 47.861 65.956 38.293 1.00 62.83 2045 N THR B 373 51.911 67.931 40.446 1.00 53.76 2046 CA THR B 373 52.915 68.766 41.085 1.00 51.64 2047 C THR B 373 52.850 70.180 40.512 1.00 48.20 2048 O THR B 373 52.801 70.355 39.296 1.00 46.65 2049 CB THR B 373 54.325 68.201 40.832 1.00 53.15 2050 OG1 THR B 373 54.324 66.789 41.073 1.00 57.77 2051 CG2 THR B 373 55.339 68.871 41.747 1.00 53.75 2052 N THR B 374 52.851 71.181 41.385 1.00 45.34 2053 CA THR B 374 52.799 72.575 40.942 1.00 44.94 2054 C THR B 374 54.161 73.259 41.041 1.00 43.68 2055 O THR B 374 54.945 72.964 41.938 1.00 42.67 2056 CB THR B 374 51.805 73.391 41.784 1.00 41.63 2057 CG THR B 374 50.371 72.977 41.657 1.00 41.50 2058 CD1 THR B 374 49.688 72.124 42.477 1.00 39.67 2059 CD2 THR B 374 49.441 73.395 40.648 1.00 35.69 2060 NE1 THR B 374 48.392 71.988 42.041 1.00 35.06 2061 CE2 THR B 374 48.214 72.756 40.922 1.00 34.53 2062 CE3 THR B 374 49.528 74.247 39.542 1.00 32.37 2063 CZ2 THR B 374 47.079 72.943 40.129 1.00 35.43 2064 CZ3 THR B 374 48.401 74.434 38.751 1.00 36.11 2065 CH2 THR B 374 47.190 73.782 39.050 1.00 37.51 2066 N SER B 375 54.430 74.179 40.119 1.00 43.53 2067 CA SER B 375 55.678 74.934 40.140 1.00 43.57 2068 C SER B 375 55.511 76.270 39.438 1.00 42.59 2069 O SER B 375 54.669 76.411 38.550 1.00 43.68 2070 CB SER B 375 56.820 74.153 39.474 1.00 45.03 2071 OG SER B 375 56.691 74.118 38.066 1.00 45.66 2072 N ARG B 376 56.299 77.251 39.866 1.00 40.79 2073 CA ARG B 376 56.279 78.569 39.266 1.00 40.12 2074 C ARG B 376 57.498 78.689 38.351 1.00 40.59 2075 O ARG B 376 58.618 78.393 38.752 1.00 40.90 2076 CB ARG B 376 56.345 79.653 40.334 1.00 40.03 2077 CG ARG B 376 55.132 79.745 41.237 1.00 43.20 2078 CD ARG B 376 54.883 81.198 41.599 1.00 41.05 2079 NE ARG B 376 55.171 81.480 42.992 1.00 50.71 2080 CZ ARG B 376 55.300 82.705 43.488 1.00 53.97 2081 NH1 ARG B 376 55.172 83.758 42.693 1.00 51.88 2082 NH2 ARG B 376 55.542 82.874 44.782 1.00 55.55 2083 N ALA B 377 57.281 79.129 37.122 1.00 40.20 2084 CA ALA B 377 58.382 79.273 36.181 1.00 40.25 2085 C ALA B 377 59.500 80.130 36.786 1.00 40.38 2086 O ALA B 377 60.657 79.979 36.422 1.00 41.16 2087 CB ALA B 377 57.879 79.903 34.878 1.00 33.12 2088 N SER B 378 59.144 81.015 37.714 1.00 40.21 2089 CA SER B 378 60.109 81.903 38.354 1.00 41.95 2090 C SER B 378 60.906 81.188 39.436 1.00 44.92 2091 O SER B 378 61.866 81.744 39.966 1.00 44.28 2092 CB SER B 378 59.401 83.096 38.992 1.00 40.91 2093 OG SER B 378 58.737 82.693 40.180 1.00 40.09 2094 N GLY B 379 60.493 79.967 39.768 1.00 46.93 2095 CA GLY B 379 61.181 79.195 40.787 1.00 49.77 2096 C GLY B 379 60.716 79.512 42.196 1.00 50.60 2097 O GLY B 379 61.024 78.783 43.142 1.00 52.95 2098 N LYS B 380 59.974 80.605 42.345 1.00 53.72 2099 CA LYS B 380 59.478 80.988 43.657 1.00 54.13 2100 C LYS B 380 58.564 79.911 44.255 1.00 48.16 2101 O LYS B 380 58.087 79.008 43.556 1.00 45.65 2102 CB LYS B 380 58.752 82.338 43.583 1.00 62.44 2103 CG LYS B 380 59.692 83.522 43.390 1.00 67.72 2104 CD LYS B 380 58.975 84.852 43.550 1.00 69.32 2105 CE LYS B 380 59.956 86.013 43.481 1.00 73.14 2106 NZ LYS B 380 59.280 87.333 43.633 1.00 77.37 2107 N PRO B 381 58.323 79.986 45.571 1.00 56.07 2108 CA PRO B 381 57.472 79.014 46.265 1.00 56.46 2109 C PRO B 381 55.993 79.065 45.875 1.00 54.32 2110 O PRO B 381 55.446 80.133 45.589 1.00 56.76 2111 CB PRO B 381 57.664 79.375 47.740 1.00 60.70 2112 CG PRO B 381 58.978 80.119 47.767 1.00 62.01 2113 CD PRO B 381 58.905 80.945 46.526 1.00 59.24 2114 N VAL B 382 55.356 77.899 45.866 1.00 55.74 2115 CA VAL B 382 53.931 77.805 45.569 1.00 55.58 2116 C VAL B 382 53.247 77.408 46.880 1.00 55.56 2117 O VAL B 382 53.848 76.734 47.720 1.00 55.22 2118 CB VAL B 382 53.620 76.726 44.493 1.00 55.39 2119 CG1 VAL B 382 54.404 77.008 43.222 1.00 55.94 2120 CG2 VAL B 382 53.936 75.339 45.025 1.00 53.06 2121 N ASN B 383 52.000 77.827 47.055 1.00 54.38 2122 CA ASN B 383 51.246 77.510 48.264 1.00 54.63 2123 C ASN B 383 50.757 76.068 48.290 1.00 53.85 2124 O ASN B 383 50.970 75.297 47.354 1.00 52.58 2125 CB ASN B 383 50.034 78.429 48.382 1.00 59.07 2126 CG ASN B 383 50.414 79.883 48.456 1.00 64.60 2127 OD1 ASN B 383 49.576 80.764 48.269 1.00 70.14 2128 ND2 ASN B 383 51.685 80.150 48.738 1.00 71.07 2129 N HIS B 384 50.094 75.710 49.381 1.00 53.46 2130 CA HIS B 384 49.543 74.371 49.526 1.00 52.22 2131 C HIS B 384 48.298 74.274 48.640 1.00 49.10 2132 O HIS B 384 47.495 75.200 48.585 1.00 45.53 2133 CB HIS B 384 49.183 74.111 50.993 1.00 59.11 2134 CG HIS B 384 50.377 73.924 51.878 1.00 62.16 2135 ND1 HIS B 384 51.243 72.862 51.739 1.00 69.15 2136 CD2 HIS B 384 50.855 74.669 52.903 1.00 70.28 2137 CE1 HIS B 384 52.206 72.960 52.639 1.00 75.01 2138 NE2 HIS B 384 51.995 74.047 53.358 1.00 74.58 2139 N SER B 385 48.146 73.152 47.949 1.00 45.07 2140 CA SER B 385 47.017 72.959 47.060 1.00 44.61 2141 C SER B 385 45.973 71.983 47.604 1.00 44.58 2142 O SER B 385 46.244 71.220 48.521 1.00 44.21 2143 CB SER B 385 47.524 72.487 45.691 1.00 44.61 2144 OG SER B 385 48.310 71.307 45.789 1.00 41.13 2145 N THR B 386 44.773 72.025 47.035 1.00 44.32 2146 CA THR B 386 43.684 71.150 47.446 1.00 44.35 2147 C THR B 386 43.444 70.113 46.363 1.00 44.09 2148 O THR B 386 43.274 70.451 45.189 1.00 44.06 2149 CB THR B 386 42.374 71.936 47.680 1.00 45.20 2150 OG1 THR B 386 42.555 72.856 48.762 1.00 51.89 2151 CG2 THR B 386 41.232 70.984 48.036 1.00 47.20 2152 N ARG B 387 43.424 68.851 46.774 1.00 44.39 2153 CA ARG B 387 43.222 67.730 45.867 1.00 46.68 2154 C ARG B 387 41.837 67.080 46.030 1.00 47.05 2155 O ARG B 387 41.372 66.850 47.149 1.00 46.65 2156 CB ARG B 387 44.316 66.694 46.121 1.00 48.13 2157 CG ARG B 387 44.270 65.488 45.210 1.00 52.77 2158 CD ARG B 387 45.106 64.353 45.780 1.00 56.60 2159 NE ARG B 387 44.978 63.141 44.979 1.00 60.65 2160 CZ ARG B 387 45.683 62.895 43.882 1.00 61.97 2161 NH1 ARG B 387 46.578 63.779 43.464 1.00 64.45 2162 NH2 ARG B 387 45.469 61.781 43.189 1.00 60.54 2163 N LYS B 388 41.185 66.780 44.910 1.00 46.93 2164 CA LYS B 388 39.870 66.143 44.933 1.00 47.51 2165 C LYS B 388 39.823 64.970 43.957 1.00 48.33 2166 O LYS B 388 40.199 65.107 42.794 1.00 46.08 2167 CB LYS B 388 38.777 67.148 44.563 1.00 46.64 2168 CG LYS B 388 38.691 68.326 45.497 1.00 52.75 2169 CD LYS B 388 37.861 69.446 44.905 1.00 58.62 2170 CE LYS B 388 38.062 70.737 45.682 1.00 62.49 2171 NZ LYS B 388 37.396 71.881 44.999 1.00 67.33 2172 N GLU B 389 39.364 63.820 44.449 1.00 50.07 2173 CA GLU B 389 39.243 62.602 43.646 1.00 51.86 2174 C GLU B 389 37.793 62.126 43.638 1.00 52.81 2175 O GLU B 389 37.192 61.917 44.695 1.00 49.21 2176 CB GLU B 389 40.126 61.494 44.223 1.00 54.67 2177 CG GLU B 389 41.616 61.710 44.044 1.00 65.65 2178 CD GLU B 389 42.441 60.608 44.688 1.00 72.66 2179 OE1 GLU B 389 42.151 59.418 44.429 1.00 75.92 2180 OE2 GLU B 389 43.380 60.931 45.450 1.00 75.78 2181 N GLU B 390 37.229 61.948 42.449 1.00 56.06 2182 CA GLU B 390 35.849 61.500 42.346 1.00 61.17 2183 C GLU B 390 35.629 60.454 41.265 1.00 64.70 2184 O GLU B 390 36.072 60.598 40.123 1.00 64.01 2185 CB GLU B 390 34.927 62.692 42.107 1.00 64.35 2186 CG GLU B 390 33.479 62.317 41.867 1.00 74.80 2187 CD GLU B 390 32.548 63.509 41.979 1.00 85.97 2188 OE1 GLU B 390 32.822 64.547 41.336 1.00 92.60 2189 OE2 GLU B 390 31.541 63.403 42.712 1.00 92.18 2190 N LYS B 391 34.921 59.396 41.639 1.00 68.18 2191 CA LYS B 391 34.640 58.312 40.712 1.00 71.58 2192 C LYS B 391 33.215 58.302 40.180 1.00 76.11 2193 O LYS B 391 32.265 58.673 40.869 1.00 75.89 2194 CB LYS B 391 34.946 56.973 41.372 1.00 67.28 2195 N GLN B 392 33.092 57.876 38.932 1.00 81.85 2196 CA CLN B 392 31.814 57.746 38.254 1.00 88.38 2197 C CLN B 392 32.026 56.482 37.443 1.00 92.30 2198 O GLN B 392 32.752 56.500 36.452 1.00 93.25 2199 CB GLN B 392 31.555 58.938 37.323 1.00 85.87 2200 CG GLN B 392 30.422 59.848 37.782 1.00 90.76 2201 CD GLN B 392 30.027 60.873 36.731 1.00 93.39 2202 OE1 GLN B 392 29.687 60.524 35.598 1.00 92.93 2203 NE2 GLN B 392 30.062 62.147 37.107 1.00 93.97 2204 N ARG B 393 31.426 55.379 37.880 1.00 96.24 2205 CA ARG B 393 31.589 54.108 37.184 1.00 100.53 2206 C ARG B 393 31.250 54.188 35.697 1.00 102.30 2207 O ARG B 393 31.273 53.178 34.993 1.00 101.15 2208 CB ARG B 393 30.747 53.021 37.855 1.00 106.99 2209 CG ARG B 393 29.251 53.196 37.704 1.00 109.77 2210 CD ARG B 393 28.521 52.107 38.464 1.00 115.73 2211 NE ARG B 393 27.095 52.085 38.165 1.00 119.73 2212 CZ ARG B 393 26.227 51.267 38.750 1.00 121.60 2213 NH1 ARG B 393 26.645 50.406 39.670 1.00 121.59 2214 NH2 ARG B 393 24.945 51.308 38.416 1.00 121.49 2215 N ASN B 394 30.942 55.391 35.224 1.00 103.98 2216 CA ASN B 394 30.630 55.595 33.819 1.00 106.60 2217 C ASN B 394 31.918 55.325 33.049 1.00 106.89 2218 O ASN B 394 31.950 54.516 32.122 1.00 108.55 2219 CB ASN B 394 30.173 57.036 33.580 1.00 108.97 2220 CG ASN B 394 29.709 57.274 32.153 1.00 112.83 2221 OD1 ASN B 394 29.459 58.410 31.752 1.00 114.53 2222 ND2 ASN B 394 29.584 56.198 31.381 1.00 114.40 2223 N GLY B 395 32.984 56.007 33.452 1.00 105.53 2224 CA GLY B 395 34.269 55.829 32.802 1.00 101.15 2225 C GLY B 395 35.177 57.015 33.050 1.00 97.82 2226 O GLY B 395 35.879 57.475 32.148 1.00 99.41 2227 N THR B 396 35.177 57.516 34.278 1.00 94.50 2228 CA THR B 396 36.011 58.663 34.578 1.00 89.02 2229 C THR B 396 36.426 58.837 36.029 1.00 83.93 2230 O THR B 396 35.600 59.123 36.896 1.00 83.27 2231 CB THR B 396 35.322 59.975 34.130 1.00 92.03 2232 OG1 THR B 396 35.116 59.952 32.712 1.00 94.17 2233 CG2 THR B 396 36.179 61.186 34.504 1.00 95.48 2234 N LEU B 397 37.718 58.658 36.279 1.00 79.69 2235 CA LEU B 397 38.280 58.871 37.600 1.00 74.75 2236 C LEU B 397 38.773 60.305 37.496 1.00 71.50 2237 O LEU B 397 39.880 60.548 37.019 1.00 74.81 2238 CB LEU B 397 39.480 57.960 37.860 1.00 75.72 2239 CG LEU B 397 40.350 58.412 39.047 1.00 70.67 2240 CD1 LEU B 397 39.742 57.932 40.362 1.00 69.05 2241 CD2 LEU B 397 41.768 57.877 38.887 1.00 72.96 2242 N THR B 398 37.941 61.252 37.905 1.00 67.61 2243 CA THR B 398 38.314 62.655 37.848 1.00 61.30 2244 C THR B 398 39.207 63.041 39.024 1.00 56.61 2245 O THR B 398 38.974 62.640 40.166 1.00 54.95 2246 CB THR B 398 37.070 63.556 37.852 1.00 61.75 2247 OG1 THR B 398 36.345 63.375 36.629 1.00 65.40 2248 CG2 THR B 398 37.471 65.016 37.992 1.00 63.39 2249 N VAL B 399 40.241 63.817 38.729 1.00 51.84 2250 CA VAL B 399 41.163 64.279 39.751 1.00 48.05 2251 C VAL B 399 41.515 65.730 39.490 1.00 44.81 2252 O VAL B 399 41.911 66.098 38.381 1.00 44.41 2253 CB VAL B 399 42.466 63.468 39.751 1.00 49.35 2254 CB1 VAL B 399 43.409 64.010 40.805 1.00 49.43 2255 CG2 VAL B 399 42.168 62.006 40.010 1.00 53.10 2256 N THR B 400 41.354 66.564 40.504 1.00 42.44 2257 CA THR B 400 41.691 67.965 40.343 1.00 40.44 2258 C THR B 400 42.532 68.449 41.498 1.00 38.07 2259 O THR B 400 42.483 67.908 42.602 1.00 36.13 2260 CB THR B 400 40.448 68.869 40.266 1.00 39.64 2261 OG1 THR B 400 39.845 68.962 41.561 1.00 43.72 2262 CG2 THR B 400 39.442 68.322 39.278 1.00 38.32 2263 N SER B 401 43.335 69.460 41.216 1.00 36.90 2264 CA SER B 401 44.168 70.069 42.224 1.00 35.46 2265 C SER B 401 43.988 71.557 42.016 1.00 33.95 2266 O SER B 401 44.153 72.062 40.908 1.00 34.80 2267 CB SER B 401 45.638 69.694 42.040 1.00 36.91 2268 OG SER B 401 46.417 70.301 43.060 1.00 40.84 2269 N THR B 402 43.635 72.248 43.086 1.00 32.28 2270 CA THR B 402 43.422 73.672 43.032 1.00 31.85 2271 C THR B 402 44.508 74.355 43.836 1.00 31.76 2272 O THR B 402 44.737 74.046 45.010 1.00 30.55 2273 CB THR B 402 42.051 74.030 43.595 1.00 31.33 2274 OG1 THR B 402 41.058 73.316 42.862 1.00 32.83 2275 CG2 THR B 402 41.782 75.522 43.468 1.00 32.70 2276 N LEU B 403 45.167 75.301 43.188 1.00 30.72 2277 CA LEU B 403 46.257 76.018 43.800 1.00 30.33 2278 C LEU B 403 45.927 77.485 44.003 1.00 29.66 2279 O LEU B 403 45.608 78.185 43.048 1.00 28.06 2280 CB LEU B 403 47.502 75.902 42.913 1.00 28.34 2281 CG LEU B 403 48.769 76.632 43.381 1.00 32.10 2282 CD1 LEU B 403 49.425 75.823 44.503 1.00 31.94 2283 CD2 LEU B 403 49.756 76.790 42.224 1.00 30.42 2284 N PRO B 404 45.983 77.962 45.259 1.00 31.48 2285 CA PRO B 404 45.704 79.367 45.566 1.00 33.20 2286 C PRO B 404 46.841 80.149 44.906 1.00 34.02 2287 O PRO B 404 47.999 79.755 44.996 1.00 32.25 2288 CB PRO B 404 45.788 79.417 47.090 1.00 33.28 2289 CG PRO B 404 45.435 78.010 47.500 1.00 31.82 2290 CD PRO B 404 46.186 77.187 46.497 1.00 31.26 2291 N VAL B 405 46.503 81.238 44.235 1.00 34.94 2292 CA VAL B 405 47.483 82.044 43.536 1.00 38.63 2293 C VAL B 405 47.541 83.472 44.068 1.00 40.02 2294 O VAL B 405 46.537 84.027 44.502 1.00 40.31 2295 CB VAL B 405 47.143 82.052 42.018 1.00 42.09 2296 CG1 VAL B 405 47.110 83.472 41.468 1.00 43.95 2297 CG2 VAL B 405 48.144 81.195 41.273 1.00 41.76 2298 N GLY B 406 48.728 84.064 44.039 1.00 42.35 2299 CA CLY B 406 48.859 85.432 44.503 1.00 43.35 2300 C GLY B 406 48.178 86.354 43.513 1.00 43.87 2301 O GLY B 406 48.286 86.154 42.303 1.00 42.68 2302 N PER B 407 47.466 87.352 44.023 1.00 44.40 2303 CA THR B 407 46.760 88.306 43.177 1.00 47.37 2304 C THR B 407 47.713 89.127 42.322 1.00 48.27 2305 O THR B 407 47.549 89.208 41.107 1.00 48.77 2306 CB THR B 407 45.922 89.288 44.022 1.00 48.44 2307 OG1 THR B 407 44.809 88.599 44.596 1.00 50.00 2308 CG2 THR B 407 45.413 90.436 43.162 1.00 53.23 2309 N ARG B 408 48.697 89.746 42.970 1.00 48.10 2310 CA ARG B 408 49.665 90.579 42.279 1.00 48.54 2311 C ARG B 408 50.540 89.773 41.335 1.00 48.48 2312 O ARG B 408 50.769 90.182 40.197 1.00 47.34 2313 CB ARG B 408 50.530 91.325 43.290 1.00 50.16 2314 N ASP B 409 51.033 88.634 41.806 1.00 48.72 2315 CA ASP B 409 51.886 87.787 40.979 1.00 50.88 2316 C ASP B 409 51.187 87.421 39.674 1.00 49.92 2317 O ASP B 409 51.789 87.468 38.598 1.00 49.76 2318 CB ASP B 409 52.260 86.512 41.738 1.00 56.18 2319 CG ASP B 409 53.013 86.801 43.026 1.00 64.80 2320 OD1 ASP B 409 54.062 87.482 42.956 1.00 71.41 2321 OD2 ASP B 409 52.561 86.353 44.105 1.00 68.29 2322 N THR B 410 49.908 87.067 39.773 1.00 48.36 2323 CA THR B 410 49.142 86.686 38.597 1.00 46.32 2324 C THR B 410 48.953 87.864 37.653 1.00 46.21 2325 O THR B 410 49.111 87.731 36.440 1.00 44.64 2326 CB THR B 410 47.774 86.120 38.992 1.00 42.82 2327 CG THR B 410 47.001 85.710 37.796 1.00 39.31 2328 CD1 THR B 410 46.104 86.467 37.103 1.00 37.29 2329 CD2 THR B 410 47.181 84.507 37.043 1.00 35.49 2330 NH1 THR B 410 45.726 85.819 35.957 1.00 39.24 2331 CE2 THR B 410 46.372 84.613 35.895 1.00 32.76 2332 CE3 THR B 410 47.956 83.351 37.228 1.00 32.07 2333 CZ2 THR B 410 46.309 83.606 34.924 1.00 29.59 2334 CZ3 THR B 410 47.896 82.352 36.269 1.00 33.68 2335 CH2 THR B 410 47.073 82.489 35.125 1.00 30.56 2336 N ILE B 411 48.611 89.016 38.212 1.00 48.11 2337 CA ILE B 411 48.408 90.209 37.401 1.00 50.90 2338 C ILE B 411 49.712 90.649 36.742 1.00 52.46 2339 O ILE B 411 49.698 91.229 35.658 1.00 53.34 2340 CB ILE B 411 47.845 91.366 38.246 1.00 51.58 2341 CG1 ILE B 411 46.456 90.987 38.770 1.00 52.81 2342 CG2 ILE B 411 47.772 92.634 37.415 1.00 51.95 2343 CD1 ILE B 411 45.823 92.034 39.669 1.00 59.38 2344 N GLU B 412 50.837 90.348 37.385 1.00 53.21 2345 CA GLU B 412 52.137 90.728 36.852 1.00 53.12 2346 C GLU B 412 52.681 89.747 35.831 1.00 51.24 2347 O GLU B 412 53.736 89.990 35.252 1.00 51.40 2348 CB GLU B 412 53.152 90.909 37.981 1.00 59.71 2349 CG GLU B 412 53.022 92.238 38.717 1.00 70.52 2350 CD GLU B 412 54.060 92.399 39.810 1.00 78.58 2351 OE1 GLU B 412 55.262 92.198 39.527 1.00 83.44 2352 OE2 GLU B 412 53.676 92.732 40.950 1.00 82.10 2353 N GLY B 413 51.982 88.634 35.623 1.00 48.47 2354 CA GLY B 413 52.427 87.677 34.626 1.00 44.62 2355 C GLY B 413 53.116 86.387 35.032 1.00 44.15 2356 O GLY B 413 53.687 85.718 34.173 1.00 43.50 2357 N GLU B 414 53.085 86.012 36.307 1.00 42.78 2358 CA GLU B 414 53.722 84.757 36.694 1.00 40.78 2359 C GLU B 414 53.105 83.652 35.851 1.00 39.97 2360 O GLU B 414 51.955 83.758 35.410 1.00 37.43 2361 CB GLU B 414 53.489 84.445 38.182 1.00 41.96 2362 CG GLU B 414 54.034 83.081 38.659 1.00 44.09 2363 CD GLU B 414 55.564 83.018 38.740 1.00 49.01 2364 OE1 GLU B 414 56.213 82.549 37.775 1.00 46.84 2365 OE2 GLU B 414 56.121 83.448 39.773 1.00 49.89 2366 N THR B 415 53.879 82.599 35.615 1.00 39.56 2367 CA THR B 415 53.403 81.464 34.847 1.00 40.76 2368 C THR B 415 53.487 80.231 35.738 1.00 40.07 2369 O THR B 415 54.533 79.960 36.323 1.00 42.10 2370 CB THR B 415 54.238 81.273 33.556 1.00 44.69 2371 OG1 THR B 415 54.222 79.893 33.171 1.00 51.98 2372 CG2 THR B 415 55.652 81.744 33.758 1.00 50.00 2373 N TYR B 416 52.380 79.500 35.860 1.00 37.57 2374 CA TYR B 416 52.327 78.318 36.714 1.00 34.50 2375 C TYR B 416 52.265 77.051 35.899 1.00 36.77 2376 O TYR B 416 51.706 77.038 34.800 1.00 35.94 2377 CB TYR B 416 51.116 78.379 37.634 1.00 34.15 2378 CG TYR B 416 51.085 79.597 38.514 1.00 30.65 2379 CD1 TYR B 416 50.777 80.856 37.992 1.00 32.53 2380 CD2 TYR B 416 51.389 79.499 39.865 1.00 31.72 2381 CE1 TYR B 416 50.772 81.984 38.803 1.00 34.27 2382 CE2 TYR B 416 51.390 80.619 40.680 1.00 32.11 2383 CZ TYR B 416 51.080 81.856 40.144 1.00 33.86 2384 OH TYR B 416 51.082 82.964 40.961 1.00 41.22 2385 N GLN B 417 52.829 75.976 36.441 1.00 37.58 2386 CA GLN B 417 52.848 74.722 35.714 1.00 39.43 2387 C GLN B 417 52.341 73.538 36.518 1.00 39.40 2388 O GLN B 417 52.664 73.373 37.694 1.00 39.63 2389 CB GLN B 417 54.269 74.421 35.211 1.00 41.37 2390 CG GLN B 417 54.350 73.214 34.278 1.00 51.81 2391 CD GLN B 417 55.773 72.856 33.886 1.00 61.69 2392 OE1 GLN B 417 56.555 72.371 34.710 1.00 67.15 2393 NE2 GLN B 417 56.119 73.096 32.621 1.00 63.64 2394 N CYS B 418 51.543 72.712 35.864 1.00 39.29 2395 CA CYS B 418 51.019 71.517 36.489 1.00 41.80 2396 C CYS B 418 51.720 70.350 35.818 1.00 42.50 2397 O CYS B 418 51.646 70.191 34.600 1.00 43.33 2398 CB CYS B 418 49.501 71.392 36.275 1.00 41.95 2399 SG CYS B 418 48.795 69.904 37.057 1.00 54.15 2400 N ARG B 419 52.418 69.551 36.609 1.00 43.98 2401 CA ARG B 419 53.103 68.375 36.093 1.00 47.51 2402 C ARG B 419 52.277 67.172 36.542 1.00 48.11 2403 O ARG B 419 52.219 66.859 37.730 1.00 47.85 2404 CB ARG B 419 54.532 68.311 36.648 1.00 49.08 2405 CG ARG B 419 55.203 66.958 36.514 1.00 54.11 2406 CD ARG B 419 56.708 67.046 36.796 1.00 64.71 2407 NE ARG B 419 57.325 65.732 36.963 1.00 64.09 2408 CZ ARG B 419 57.437 65.107 38.132 1.00 70.31 2409 NH1 ARG B 419 56.981 65.681 39.239 1.00 68.32 2410 NH2 ARG B 419 57.992 63.901 38.195 1.00 71.53 2411 N VAL B 420 51.610 66.524 35.592 1.00 51.04 2412 CA VAL B 420 50.776 65.369 35.900 1.00 56.22 2413 C VAL B 420 51.561 64.068 35.746 1.00 61.25 2414 O VAL B 420 52.178 63.820 34.707 1.00 60.11 2415 CB VAL B 420 49.536 65.305 34.985 1.00 54.44 2416 CG1 VAL B 420 48.678 64.106 35.371 1.00 52.69 2417 CG2 VAL B 420 48.732 66.597 35.095 1.00 55.45 2418 N THR B 421 51.529 63.241 36.786 1.00 66.23 2419 CA THR B 421 52.244 61.969 36.774 1.00 73.18 2420 C THR B 421 51.334 60.766 36.970 1.00 76.87 2421 O THR B 421 50.968 60.443 38.100 1.00 77.93 2422 CB THR B 421 53.317 61.929 37.875 1.00 73.75 2423 OG1 THR B 421 54.272 62.972 37.649 1.00 77.71 2424 CG2 THR B 421 54.033 60.591 37.873 1.00 75.35 2425 N HIS B 422 50.976 60.101 35.874 1.00 81.02 2426 CA HIS B 422 50.117 58.922 35.949 1.00 86.07 2427 C HIS B 422 51.004 57.686 35.822 1.00 89.67 2428 O HIS B 422 51.920 57.653 35.002 1.00 90.00 2429 CB HIS B 422 49.071 58.940 34.831 1.00 87.43 2430 CG HIS B 422 47.892 58.052 35.092 1.00 90.73 2431 ND1 HIS B 422 47.076 58.203 36.191 1.00 93.83 2432 CD2 HIS B 422 47.396 57.000 34.396 1.00 91.89 2433 CE1 HIS B 422 46.127 57.282 36.164 1.00 94.70 2434 NE2 HIS B 422 46.300 56.540 35.085 1.00 93.25 2435 N PRO B 423 50.729 56.646 36.626 1.00 92.64 2436 CA PRO B 423 51.489 55.391 36.640 1.00 95.19 2437 C PRO B 423 51.972 54.762 35.325 1.00 97.06 2438 O PRO B 423 53.169 54.536 35.155 1.00 97.57 2439 CB PRO B 423 50.576 54.445 37.433 1.00 95.56 2440 CG PRO B 423 49.209 55.034 37.247 1.00 93.94 2441 CD PRO B 423 49.488 56.495 37.404 1.00 93.12 2442 N HIS B 424 51.058 54.495 34.399 1.00 98.71 2443 CA HIS B 424 51.410 53.831 33.143 1.00 100.16 2444 C HIS B 424 52.104 54.579 32.005 1.00 99.67 2445 O HIS B 424 52.910 53.991 31.284 1.00 99.61 2446 CB HIS B 424 50.165 53.149 32.578 1.00 102.42 2447 CG HIS B 424 49.578 52.125 33.495 1.00 105.47 2448 ND1 HIS B 424 48.302 52.228 34.008 1.00 107.10 2449 CD2 HIS B 424 50.079 50.961 33.967 1.00 97.46 2450 CE1 HIS B 424 48.044 51.170 34.755 1.00 106.81 2451 NE2 HIS B 424 49.106 50.385 34.747 1.00 106.61 2452 N LEU B 425 51.802 55.858 31.833 1.00 99.19 2453 CA LEU B 425 52.384 56.628 30.737 1.00 99.01 2454 C LEU B 425 53.886 56.908 30.816 1.00 98.36 2455 O LEU B 425 54.440 57.121 31.896 1.00 98.39 2456 CB LEU B 425 51.606 57.929 30.593 1.00 100.66 2457 CG LEU B 425 50.105 57.631 30.633 1.00 101.95 2458 CD1 LEU B 425 49.315 58.917 30.531 1.00 102.59 2459 CD2 LEU B 425 49.744 56.677 29.502 1.00 103.85 2460 N PRO B 426 54.562 56.915 29.652 1.00 97.57 2461 CA PRO B 426 56.004 57.165 29.560 1.00 96.82 2462 C PRO B 426 56.414 58.525 30.108 1.00 95.53 2463 O PRO B 426 57.040 58.610 31.163 1.00 95.77 2464 CB PRO B 426 56.282 57.030 28.063 1.00 97.13 2465 CG PRO B 426 54.995 57.494 27.440 1.00 97.88 2466 CD PRO B 426 53.969 56.798 28.307 1.00 97.70 2467 N ARG B 427 56.064 59.585 29.387 1.00 94.16 2468 CA ARG B 427 56.402 60.931 29.826 1.00 92.52 2469 C ARG B 427 55.285 61.509 30.692 1.00 89.85 2470 O ARG B 427 54.123 61.113 30.583 1.00 89.26 2471 CB ARG B 427 56.652 61.851 28.622 1.00 97.34 2472 CG ARG B 427 57.202 63.219 29.023 1.00 99.32 2473 CD ARG B 427 57.407 64.172 27.847 1.00 105.99 2474 NE ARG B 427 58.068 65.403 28.285 1.00 111.10 2475 CZ ARG B 427 58.302 66.460 27.512 1.00 111.66 2476 NH1 ARG B 427 57.927 66.457 26.239 1.00 111.70 2477 NH2 ARG B 427 58.921 67.522 28.013 1.00 110.09 2478 N ALA B 428 55.651 62.442 31.562 1.00 86.56 2479 CA ALA B 428 54.690 63.087 32.439 1.00 82.70 2480 C ALA B 428 53.998 64.211 31.677 1.00 80.03 2481 O ALA B 428 54.619 64.889 30.861 1.00 80.29 2482 CB ALA B 428 55.400 63.647 33.663 1.00 83.85 2483 N LEU B 429 52.708 64.397 31.936 1.00 76.76 2484 CA LEU B 429 51.949 65.456 31.285 1.00 72.72 2485 C LEU B 429 52.311 66.780 31.936 1.00 69.67 2486 O LEU B 429 52.472 66.858 33.153 1.00 68.64 2487 CB LEU B 429 50.444 65.208 31.429 1.00 73.60 2488 CG LEU B 429 49.753 64.431 30.307 1.00 73.35 2489 CD1 LEU B 429 48.320 64.102 30.696 1.00 72.09 2490 CD2 LEU B 429 49.787 65.267 29.035 1.00 76.40 2491 N MET B 430 52.447 67.821 31.124 1.00 66.83 2492 CA MET B 430 52.786 69.132 31.651 1.00 64.81 2493 C MET B 430 51.922 70.216 31.026 1.00 61.41 2494 O MET B 430 51.824 70.326 29.801 1.00 60.84 2495 CB MET B 430 54.265 69.427 31.409 1.00 68.22 2496 CG MET B 430 55.184 68.353 31.967 1.00 74.39 2497 SD MET B 430 56.921 68.714 31.713 1.00 83.18 2498 CE MET B 430 56.993 68.764 29.906 1.00 84.12 2499 N ARG B 431 51.288 71.010 31.882 1.00 57.17 2500 CA ARG B 431 50.428 72.094 31.426 1.00 54.04 2501 C ARG B 431 50.848 73.366 32.137 1.00 50.58 2502 O ARG B 431 51.233 73.330 33.304 1.00 50.46 2503 CB ARG B 431 48.959 71.775 31.736 1.00 55.16 2504 CG ARG B 431 48.413 70.564 30.991 1.00 59.24 2505 CD ARG B 431 48.428 70.798 29.489 1.00 63.93 2506 NE ARG B 431 48.014 69.617 28.737 1.00 70.30 2507 CZ ARG B 431 48.043 69.530 27.411 1.00 76.24 2508 NH1 ARG B 431 48.469 70.559 26.683 1.00 77.83 2509 NH2 ARG B 431 47.648 68.415 26.811 1.00 77.12 2510 N SER B 432 50.788 74.488 31.431 1.00 46.92 2511 CA SER B 432 51.163 75.765 32.016 1.00 45.15 2512 C SER B 432 50.118 76.816 31.702 1.00 42.49 2513 O SER B 432 49.382 76.699 30.721 1.00 42.76 2514 CB SER B 432 52.532 76.206 31.490 1.00 44.31 2515 OG SER B 432 52.516 76.284 30.082 1.00 49.96 2516 N THR B 433 50.060 77.851 32.530 1.00 40.28 2517 CA THR B 433 49.078 78.909 32.337 1.00 39.71 2518 C THR B 433 49.604 80.244 32.843 1.00 39.49 2519 O THR B 433 50.414 80.285 33.766 1.00 40.22 2520 CB THR B 433 47.761 78.577 33.078 1.00 38.07 2521 OG1 THR B 433 46.793 79.594 32.805 1.00 39.56 2522 CG2 THR B 433 47.991 78.512 34.582 1.00 36.99 2523 N THR B 434 49.139 81.328 32.226 1.00 39.18 2524 CA THR B 434 49.532 82.687 32.588 1.00 40.70 2525 C THR B 434 48.414 83.635 32.166 1.00 40.23 2526 O THR B 434 47.509 83.236 31.441 1.00 41.18 2527 CB THR B 434 50.816 83.116 31.844 1.00 43.01 2528 OG1 THR B 434 50.548 83.238 30.439 1.00 47.85 2529 CG2 THR B 434 51.874 82.076 31.995 1.00 48.67 2530 N LYS B 435 48.475 84.886 32.604 1.00 40.97 2531 CA LYS B 435 47.450 85.833 32.211 1.00 45.73 2532 C LYS B 435 47.579 85.999 30.702 1.00 48.93 2533 O LYS B 435 48.670 85.890 30.158 1.00 48.49 2534 CB LYS B 435 47.663 87.166 32.906 1.00 45.94 2535 N THR B 436 46.467 86.235 30.018 1.00 52.01 2536 CA THR B 436 46.520 86.429 28.574 1.00 54.88 2537 C THR B 436 46.916 87.878 28.326 1.00 55.70 2538 O THR B 436 46.454 88.777 29.023 1.00 55.21 2539 CB THR B 436 45.146 86.162 27.909 1.00 56.24 2540 OG1 THR B 436 44.798 84.779 28.062 1.00 60.56 2541 CG2 THR B 436 45.188 86.510 26.423 1.00 57.04 2542 N SER B 437 47.790 88.099 27.352 1.00 57.93 2543 CA SER B 437 48.220 89.451 27.020 1.00 60.42 2544 C SER B 437 47.361 89.917 25.851 1.00 60.49 2545 O SER B 437 46.397 89.243 25.477 1.00 60.21 2546 CB SER B 437 49.706 89.467 26.630 1.00 61.57 2547 OG SER B 437 49.949 88.643 25.500 1.00 65.51 2548 N GLY B 438 47.705 91.067 25.279 1.00 60.09 2549 CA GLY B 438 46.934 91.578 24.161 1.00 58.42 2550 C GLY B 438 45.970 92.663 24.589 1.00 57.80 2551 O GLY B 438 45.853 92.952 25.778 1.00 56.51 2552 N PRO B 439 45.267 93.291 23.633 1.00 57.81 2553 CA PRO B 439 44.305 94.358 23.915 1.00 56.19 2554 C PRO B 439 43.178 93.908 24.837 1.00 53.91 2555 O PRO B 439 42.891 92.714 24.953 1.00 53.91 2556 CB PRO B 439 43.794 94.735 22.524 1.00 57.79 2557 CG PRO B 439 44.967 94.453 21.652 1.00 58.60 2558 CD PRO B 439 45.427 93.115 22.179 1.00 60.65 2559 N ARG B 440 42.545 94.878 25.488 1.00 51.09 2560 CA ARG B 440 41.437 94.610 26.398 1.00 48.90 2561 C ARG B 440 40.235 95.380 25.869 1.00 45.83 2562 O ARG B 440 40.398 96.412 25.219 1.00 45.88 2563 CB ARG B 440 41.764 95.099 27.811 1.00 49.95 2564 CG ARG B 440 43.127 94.681 28.329 1.00 59.03 2565 CD ARG B 440 43.227 93.194 28.652 1.00 65.31 2566 NE ARG B 440 44.627 92.786 28.758 1.00 72.31 2567 CZ ARG B 440 45.047 91.614 29.222 1.00 74.99 2568 NH1 ARG B 440 44.181 90.706 29.640 1.00 77.22 2569 NH2 ARG B 440 46.345 91.348 29.263 1.00 78.59 2570 N ALA B 441 39.036 94.873 26.143 1.00 42.09 2571 CA ALA B 441 37.800 95.521 25.713 1.00 39.26 2572 C ALA B 441 36.706 95.124 26.687 1.00 38.22 2573 O ALA B 441 36.566 93.951 27.024 1.00 38.95 2574 CB ALA B 441 37.430 95.089 24.302 1.00 36.56 2575 N ALA B 442 35.934 96.104 27.134 1.00 37.22 2576 CA ALA B 442 34.871 95.861 28.089 1.00 37.60 2577 C ALA B 442 33.721 95.050 27.510 1.00 38.65 2578 O ALA B 442 33.497 95.047 26.302 1.00 40.22 2579 CB ALA B 442 34.352 97.185 28.619 1.00 37.17 2580 N PRO B 443 32.981 94.340 28.378 1.00 38.04 2581 CA PRO B 443 31.835 93.511 27.996 1.00 36.79 2582 C PRO B 443 30.581 94.376 27.857 1.00 38.14 2583 O PRO B 443 30.426 95.364 28.579 1.00 37.39 2584 CB PRO B 443 31.677 92.550 29.179 1.00 36.30 2585 CG PRO B 443 32.968 92.654 29.941 1.00 36.35 2586 CD PRO B 443 33.351 94.088 29.780 1.00 37.85 2587 N GLU B 444 29.706 94.006 26.927 1.00 36.28 2588 CA GLU B 444 28.437 94.699 26.729 1.00 35.57 2589 C GLU B 444 27.429 93.659 27.212 1.00 33.87 2590 O GLU B 444 27.495 92.490 26.809 1.00 33.43 2591 CB GLU B 444 28.217 95.020 25.249 1.00 38.68 2592 N VAL B 445 26.503 94.080 28.067 1.00 30.18 2593 CA VAL B 445 25.530 93.168 28.650 1.00 28.24 2594 C VAL B 445 24.077 93.464 28.289 1.00 28.44 2595 O VAL B 445 23.625 94.600 28.379 1.00 26.78 2596 CB VAL B 445 25.663 93.183 30.195 1.00 28.10 2597 CG1 VAL B 445 24.667 92.230 30.826 1.00 25.56 2598 CG2 VAL B 445 27.079 92.829 30.589 1.00 26.30 2599 N TYR B 446 23.349 92.425 27.897 1.00 27.87 2600 CA TYR B 446 21.949 92.581 27.549 1.00 27.91 2601 C TYR B 446 21.140 91.407 28.076 1.00 27.06 2602 O TYR B 446 21.293 90.274 27.620 1.00 27.96 2603 CB TYR B 446 21.764 92.702 26.026 1.00 26.45 2604 CG TYR B 446 20.311 92.851 25.653 1.00 26.59 2605 CD1 TYR B 446 19.543 93.886 26.195 1.00 28.48 2606 CD2 TYR B 446 19.686 91.941 24.795 1.00 29.02 2607 CE1 TYR B 446 18.183 94.011 25.896 1.00 33.24 2608 CE2 TYR B 446 18.326 92.057 24.484 1.00 31.33 2609 CZ TYR B 446 17.585 93.094 25.041 1.00 36.01 2610 OH TYR B 446 16.248 93.213 24.762 1.00 36.54 2611 N ALA B 447 20.274 91.686 29.040 1.00 28.07 2612 CA ALA B 447 19.450 90.651 29.661 1.00 27.67 2613 C ALA B 447 18.021 90.785 29.168 1.00 29.19 2614 O ALA B 447 17.564 91.898 28.927 1.00 31.10 2615 CB ALA B 447 19.502 90.798 31.169 1.00 23.97 2616 N PHE B 448 17.307 89.671 29.021 1.00 29.56 2617 CA PHE B 448 15.943 89.751 28.522 1.00 32.50 2618 C PHE B 448 15.117 88.525 28.854 1.00 33.67 2619 O PHE B 448 15.650 87.488 29.228 1.00 35.26 2620 CB PHE B 448 15.970 89.941 27.003 1.00 35.29 2621 CG PHE B 448 16.523 88.751 26.262 1.00 37.04 2622 CD1 PHE B 448 15.691 87.688 25.905 1.00 36.66 2623 CD2 PHE B 448 17.886 88.666 25.973 1.00 34.95 2624 CE1 PHE B 448 16.218 86.551 25.276 1.00 40.91 2625 CE2 PHE B 448 18.422 87.534 25.347 1.00 35.99 2626 CZ PHE B 448 17.586 86.477 24.997 1.00 35.15 2627 N ALA B 449 13.804 88.648 28.704 1.00 35.81 2628 CA ALA B 449 12.907 87.534 28.969 1.00 37.63 2629 C ALA B 449 12.347 86.983 27.662 1.00 40.96 2630 O ALA B 449 12.159 87.715 26.697 1.00 40.14 2631 CB ALA B 449 11.769 87.977 29.870 1.00 33.60 2632 N THR B 450 12.091 85.682 27.652 1.00 45.40 2633 CA THR B 450 11.529 84.994 26.505 1.00 50.82 2634 C THR B 450 10.003 85.085 26.602 1.00 53.78 2635 O THR B 450 9.431 84.927 27.683 1.00 54.14 2636 CB THR B 450 11.935 83.510 26.513 1.00 51.45 2637 OG1 THR B 450 13.358 83.408 26.650 1.00 54.12 2638 CG2 THR B 450 11.507 82.831 25.223 1.00 55.58 2639 N PRO B 451 9.325 85.340 25.474 1.00 56.74 2640 CA PRO B 451 7.863 85.443 25.477 1.00 59.05 2641 C PRO B 451 7.209 84.173 26.020 1.00 61.00 2642 O PRO B 451 7.520 83.065 25.579 1.00 59.71 2643 CB PRO B 451 7.527 85.667 24.002 1.00 60.52 2644 CG PRO B 451 8.749 86.338 23.460 1.00 61.14 2645 CD PRO B 451 9.861 85.551 24.119 1.00 59.39 2646 N GLU B 452 6.315 84.328 26.988 1.00 64.30 2647 CA GLU B 452 5.625 83.172 27.542 1.00 69.17 2648 C GLU B 452 4.137 83.348 27.258 1.00 72.61 2649 O GLU B 452 3.394 83.933 28.043 1.00 73.59 2650 CB GLU B 452 5.888 83.040 29.046 1.00 65.66 2651 CG GLU B 452 6.034 81.585 29.523 1.00 61.46 2652 CD GLU B 452 7.283 80.883 28.967 1.00 60.52 2653 OE1 GLU B 452 8.336 81.547 28.849 1.00 63.47 2654 OE2 GLU B 452 7.227 79.666 28.667 1.00 53.34 2655 N THR B 453 3.731 82.837 26.103 1.00 76.75 2656 CA THR B 453 2.358 82.907 25.619 1.00 81.00 2657 C THR B 453 1.573 81.714 26.187 1.00 82.30 2658 O THR B 453 1.890 80.562 25.885 1.00 82.08 2659 CB THR B 453 2.409 82.863 24.090 1.00 85.65 2660 CG THR B 453 1.233 83.418 23.366 1.00 89.76 2661 CD1 THR B 453 0.679 84.661 23.512 1.00 92.34 2662 CD2 THR B 453 0.517 82.781 22.305 1.00 94.15 2663 NH1 THR B 453 −0.334 84.836 22.598 1.00 94.99 2664 CE2 THR B 453 −0.455 83.696 21.845 1.00 95.56 2665 CE3 THR B 453 0.605 81.521 21.693 1.00 95.36 2666 CZ2 THR B 453 −1.335 83.392 20.800 1.00 97.14 2667 CZ3 THR B 453 −0.269 81.220 20.655 1.00 95.61 2668 CH2 THR B 453 −1.226 82.153 20.220 1.00 97.12 2669 N PRO B 454 0.542 81.981 27.020 1.00 84.10 2670 CA PRO B 454 −0.331 80.994 27.678 1.00 87.24 2671 C PRO B 454 −0.716 79.708 26.938 1.00 90.52 2672 O PRO B 454 −0.378 79.512 25.767 1.00 89.75 2673 CB PRO B 454 −1.550 81.825 28.112 1.00 84.91 2674 CG PRO B 454 −1.417 83.125 27.360 1.00 83.62 2675 CD PRO B 454 0.063 83.341 27.307 1.00 84.60 2676 N GLY B 455 −1.455 78.849 27.636 1.00 91.72 2677 CA GLY B 455 −1.813 77.552 27.088 1.00 94.13 2678 C GLY B 455 −0.532 76.870 27.499 1.00 96.28 2679 O CLY B 455 0.475 76.987 26.799 1.00 97.74 2680 N SER B 456 −0.542 76.158 28.622 1.00 99.11 2681 CA SER B 456 0.731 75.626 29.077 1.00 96.15 2682 C SER B 456 1.135 74.193 29.424 1.00 91.50 2683 O SER B 456 0.316 73.308 29.767 1.00 88.52 2684 CB SER B 456 1.222 76.508 30.221 1.00 95.05 2685 OG SER B 456 0.225 76.690 31.216 1.00 110.76 2686 N ARG B 457 2.464 74.059 29.348 1.00 87.73 2687 CA ARG B 457 3.349 72.936 29.580 1.00 87.81 2688 C ARG B 457 4.497 73.922 29.453 1.00 86.30 2689 O ARG B 457 4.602 74.574 28.403 1.00 90.57 2690 CB ARG B 457 3.339 71.966 28.425 1.00 94.67 2691 N ASP B 458 5.341 74.088 30.473 1.00 87.32 2692 CA ASP B 458 6.314 75.159 30.320 1.00 80.43 2693 C ASP B 458 7.637 75.178 31.020 1.00 72.83 2694 O ASP B 458 8.163 74.190 31.501 1.00 73.96 2695 CB ASP B 458 5.615 76.450 30.715 1.00 83.19 2696 CG ASP B 458 5.300 76.498 32.210 1.00 85.09 2697 OD1 ASP B 458 4.694 75.535 32.722 1.00 91.25 2698 OD2 ASP B 458 5.661 77.492 32.883 1.00 90.84 2699 N LYS B 459 8.149 76.404 31.024 1.00 66.05 2700 CA LYS B 459 9.389 76.818 31.663 1.00 61.75 2701 C LYS B 459 9.617 78.232 31.214 1.00 56.14 2702 O LYS B 459 9.952 78.456 30.054 1.00 56.54 2703 CB LYS B 459 10.569 75.959 31.211 1.00 68.18 2704 CG LYS B 459 10.796 74.799 32.131 1.00 71.85 2705 CD LYS B 459 10.737 75.194 33.601 1.00 73.79 2706 CE LYS B 459 10.761 73.945 34.474 1.00 76.14 2707 NZ LYS B 459 10.925 74.259 35.931 1.00 79.35 2708 N ARG B 460 9.406 79.194 32.099 1.00 52.32 2709 CA ARG B 460 9.649 80.565 31.723 1.00 47.59 2710 C ARG B 460 11.164 80.740 31.810 1.00 43.34 2711 O ARG B 460 11.839 80.123 32.638 1.00 40.40 2712 CB ARG B 460 8.874 81.496 32.644 1.00 49.27 2713 CG ARG B 460 7.384 81.325 32.429 1.00 56.23 2714 CD ARG B 460 6.594 81.941 33.568 1.00 63.20 2715 NE ARG B 460 5.174 81.603 33.504 1.00 68.02 2716 CZ ARG B 460 4.645 80.455 33.920 1.00 70.46 2717 NH1 ARG B 460 5.415 79.506 34.444 1.00 72.23 2718 NH2 ARG B 460 3.336 80.264 33.815 1.00 73.53 2719 N THR B 461 11.690 81.538 30.902 1.00 39.19 2720 CA THR B 461 13.126 81.721 30.822 1.00 36.81 2721 C THR B 461 13.596 83.153 30.699 1.00 34.03 2722 O THR B 461 12.993 83.969 29.990 1.00 33.96 2723 CB THR B 461 13.710 80.997 29.588 1.00 39.13 2724 OG1 THR B 461 13.243 79.643 29.543 1.00 46.04 2725 CG2 THR B 461 15.220 80.970 29.679 1.00 45.48 2726 N LEU B 462 14.696 83.443 31.386 1.00 29.84 2727 CA LEU B 462 15.333 84.747 31.312 1.00 28.03 2728 C LEU B 462 16.674 84.395 30.690 1.00 27.33 2729 O LEU B 462 17.186 83.293 30.893 1.00 24.47 2730 CB LEU B 462 15.526 85.377 32.697 1.00 25.97 2731 CG LEU B 462 14.238 85.712 33.465 1.00 33.39 2732 CD1 LEU B 462 14.593 86.428 34.781 1.00 32.36 2733 CD2 LEU B 462 13.337 86.586 32.617 1.00 30.72 2734 N ALA B 463 17.241 85.314 29.922 1.00 25.83 2735 CA ALA B 463 18.489 85.023 29.264 1.00 25.65 2736 C ALA B 463 19.321 86.270 29.143 1.00 26.32 2737 O ALA B 463 18.810 87.386 29.254 1.00 27.53 2738 CB ALA B 463 18.219 84.421 27.888 1.00 28.15 2739 N CYS B 464 20.608 86.082 28.905 1.00 21.23 2740 CA CYS B 464 21.507 87.212 28.824 1.00 24.77 2741 C CYS B 464 22.584 87.001 27.786 1.00 22.14 2742 O CYS B 464 23.169 85.917 27.698 1.00 24.66 2743 CB CYS B 464 22.171 87.407 30.186 1.00 22.04 2744 SG CYS B 464 23.302 88.810 30.380 1.00 34.06 2745 N LEU B 465 22.859 88.052 27.025 1.00 22.44 2746 CA LEU B 465 23.903 88.002 26.011 1.00 23.11 2747 C LEU B 465 24.985 88.956 26.459 1.00 22.43 2748 O LEU B 465 24.702 90.117 26.748 1.00 23.73 2749 CB LEU B 465 23.370 88.445 24.639 1.00 22.99 2750 CG LEU B 465 24.423 88.790 23.562 1.00 19.04 2751 CD1 LEU B 465 25.269 87.565 23.234 1.00 21.72 2752 CD2 LEU B 465 23.716 89.253 22.282 1.00 28.23 2753 N ILE B 466 26.220 88.475 26.519 1.00 22.56 2754 CA ILE B 466 27.332 89.323 26.931 1.00 22.11 2755 C ILE B 466 28.344 89.298 25.803 1.00 24.25 2756 O ILE B 466 28.785 88.225 25.394 1.00 24.93 2757 CB ILE B 466 27.946 88.819 28.239 1.00 22.15 2758 CG1 ILE B 466 26.850 88.751 29.314 1.00 23.07 2759 CG2 ILE B 466 29.075 89.778 28.684 1.00 25.24 2760 CD1 ILE B 466 27.282 88.091 30.604 1.00 33.12 2761 N GLN B 467 28.737 90.468 25.307 1.00 24.63 2762 CA GLN B 467 29.630 90.480 24.149 1.00 28.64 2763 C GLN B 467 30.637 91.618 24.028 1.00 31.08 2764 O GLN B 467 30.685 92.529 24.865 1.00 31.00 2765 CB GLN B 467 28.770 90.428 22.872 1.00 25.58 2766 CG GLN B 467 27.873 91.657 22.696 1.00 25.53 2767 CD GLN B 467 26.907 91.556 21.501 1.00 30.72 2768 OE1 GLN B 467 27.144 90.810 20.551 1.00 29.76 2769 NE2 GLN B 467 25.821 92.327 21.550 1.00 32.18 2770 N ASN B 468 31.453 91.517 22.977 1.00 33.71 2771 CA ASN B 468 32.494 92.486 22.641 1.00 36.96 2772 C ASN B 468 33.601 92.607 23.677 1.00 38.20 2773 O ASN B 468 34.208 93.669 23.812 1.00 38.39 2774 CB ASN B 468 31.881 93.869 22.424 1.00 41.06 2775 CG ASN B 468 30.763 93.852 21.414 1.00 46.41 2776 OD1 ASN B 468 30.879 93.228 20.359 1.00 50.82 2777 ND2 ASN B 468 29.672 94.548 21.724 1.00 53.31 2778 N PHE B 469 33.868 91.535 24.415 1.00 35.74 2779 CA PHE B 469 34.910 91.597 25.423 1.00 33.87 2780 C PHE B 469 36.147 90.796 25.044 1.00 33.63 2781 O PHE B 469 36.087 89.873 24.240 1.00 34.78 2782 CB PHE B 469 34.372 91.105 26.778 1.00 29.12 2783 CG PHE B 469 33.909 89.674 26.766 1.00 26.27 2784 CD1 PHE B 469 34.808 88.641 26.967 1.00 22.45 2785 CD2 PHE B 469 32.566 89.362 26.561 1.00 22.06 2786 CE1 PHE B 469 34.386 87.315 26.974 1.00 23.84 2787 CE2 PHE B 469 32.135 88.036 26.564 1.00 28.02 2788 CZ PHE B 469 33.051 87.007 26.773 1.00 23.33 2789 N MET B 470 37.273 91.169 25.634 1.00 35.64 2790 CA MET B 470 38.535 90.480 25.413 1.00 37.62 2791 C MET B 470 39.496 90.916 26.504 1.00 36.36 2792 O MET B 470 39.478 92.071 26.923 1.00 36.33 2793 CB MET B 470 39.105 90.796 24.024 1.00 42.61 2794 CG MET B 470 39.421 92.246 23.750 1.00 50.60 2795 SD MET B 470 39.856 92.459 21.987 1.00 66.08 2796 CE MET B 470 41.544 91.820 21.966 1.00 66.35 2797 N PRO B 471 40.317 89.987 27.021 1.00 34.63 2798 CA PRO B 471 40.431 88.561 26.682 1.00 32.61 2799 C PRO B 471 39.147 87.782 26.957 1.00 31.92 2800 O PRO B 471 38.164 88.356 27.415 1.00 29.59 2801 CB PRO B 471 41.585 88.080 27.562 1.00 33.95 2802 CG PRO B 471 42.373 89.323 27.805 1.00 37.90 2803 CD PRO B 471 41.309 90.354 28.042 1.00 34.78 2804 N GLU B 472 39.187 86.472 26.714 1.00 32.28 2805 CA GLU B 472 38.020 85.599 26.866 1.00 36.49 2806 C GLU B 472 37.557 85.220 28.270 1.00 35.52 2807 O GLU B 472 36.438 84.730 28.417 1.00 34.87 2808 CB GLU B 472 38.223 84.298 26.085 1.00 41.97 2809 CG GLU B 472 39.294 83.387 26.677 1.00 54.78 2810 CD GLU B 472 39.456 82.073 25.916 1.00 62.41 2811 OE1 GLU B 472 39.021 81.997 24.744 1.00 67.26 2812 OE2 GLU B 472 40.034 81.119 26.487 1.00 64.96 2813 N ASP B 473 38.379 85.439 29.295 1.00 34.38 2814 CA ASP B 473 37.971 85.057 30.648 1.00 31.83 2815 C ASP B 473 36.914 85.998 31.214 1.00 31.24 2816 O ASP B 473 37.072 87.220 31.199 1.00 31.80 2817 CB ASP B 473 39.180 84.979 31.584 1.00 34.73 2818 CG ASP B 473 40.147 83.854 31.196 1.00 40.83 2819 OD1 ASP B 473 39.676 82.759 30.804 1.00 44.18 2820 OD2 ASP B 473 41.378 84.061 31.290 1.00 40.17 2821 N ILE B 474 35.826 85.416 31.702 1.00 26.96 2822 CA ILE B 474 34.744 86.207 32.246 1.00 25.39 2823 C ILE B 474 33.885 85.375 33.208 1.00 24.74 2824 O ILE B 474 33.776 84.164 33.069 1.00 25.20 2825 CB ILE B 474 33.862 86.758 31.092 1.00 23.81 2826 CG1 ILE B 474 32.925 87.852 31.598 1.00 22.23 2827 CG2 ILE B 474 33.062 85.626 30.453 1.00 27.10 2828 CD1 ILE B 474 32.144 88.536 30.450 1.00 25.30 2829 N SER B 475 33.312 86.030 34.209 1.00 23.27 2830 CA SER B 475 32.430 85.348 35.148 1.00 22.17 2831 C SER B 475 31.066 85.991 34.952 1.00 21.71 2832 O SER B 475 30.951 87.207 34.876 1.00 20.84 2833 CB SER B 475 32.879 85.551 36.593 1.00 20.43 2834 OG SER B 475 34.164 85.011 36.806 1.00 30.00 2835 N VAL B 476 30.042 85.158 34.887 1.00 21.76 2836 CA VAL B 476 28.694 85.620 34.675 1.00 21.72 2837 C VAL B 476 27.875 85.165 35.851 1.00 23.56 2838 O VAL B 476 28.036 84.045 36.320 1.00 25.95 2839 CB VAL B 476 28.087 84.994 33.385 1.00 21.56 2840 CG1 VAL B 476 26.625 85.443 33.222 1.00 18.70 2841 CG2 VAL B 476 28.915 85.403 32.166 1.00 20.99 2842 N GLN B 477 26.994 86.026 36.336 1.00 25.16 2843 CA GLN B 477 26.172 85.635 37.460 1.00 26.65 2844 C GLN B 477 24.833 86.337 37.438 1.00 26.62 2845 O GLN B 477 24.709 87.440 36.925 1.00 26.40 2846 CB GLN B 477 26.917 85.899 38.775 1.00 31.51 2847 CG GLN B 477 27.348 87.311 39.011 1.00 44.27 2848 CD GLN B 477 28.505 87.412 40.016 1.00 47.76 2849 OE1 GLN B 477 28.814 88.496 40.502 1.00 50.57 2850 NE2 GLN B 477 29.151 86.283 40.313 1.00 47.32 2851 N THR B 478 23.820 85.659 37.954 1.00 27.41 2852 CA THR B 478 22.488 86.225 38.026 1.00 28.36 2853 C THR B 478 22.192 86.656 39.465 1.00 30.10 2854 O THR B 478 22.660 86.033 40.428 1.00 25.31 2855 CB THR B 478 21.461 85.196 37.567 1.00 28.76 2856 CG THR B 478 21.502 84.951 36.087 1.00 34.11 2857 CD1 THR B 478 22.313 84.078 35.415 1.00 31.25 2858 CD2 THR B 478 20.722 85.620 35.094 1.00 31.01 2859 NE1 THR B 478 22.085 84.164 34.069 1.00 27.71 2860 CE2 THR B 478 21.113 85.104 33.841 1.00 31.95 2861 CE3 THR B 478 19.729 86.607 35.140 1.00 34.16 2862 CZ2 THR B 478 20.542 85.545 32.637 1.00 25.26 2863 CZ3 THR B 478 19.161 87.044 33.947 1.00 31.64 2864 CH2 THR B 478 19.571 86.511 32.713 1.00 28.89 2865 N LEU B 479 21.418 87.723 39.602 1.00 32.48 2866 CA LEU B 479 21.049 88.245 40.913 1.00 37.36 2867 C LEU B 479 19.584 88.657 40.960 1.00 40.42 2868 O LEU B 479 19.040 89.152 39.977 1.00 40.14 2869 CB LEU B 479 21.878 89.478 41.252 1.00 39.83 2870 CG LEU B 479 23.346 89.556 40.842 1.00 44.57 2871 CD1 LEU B 479 23.890 90.887 41.290 1.00 52.98 2872 CD2 LEU B 479 24.130 88.439 41.466 1.00 50.71 2873 N HIS B 480 18.947 88.448 42.102 1.00 43.05 2874 CA HIS B 480 17.572 88.877 42.276 1.00 49.20 2875 C HIS B 480 17.746 90.136 43.116 1.00 52.73 2876 O HIS B 480 17.705 90.091 44.347 1.00 52.90 2877 CB HIS B 480 16.754 87.844 43.043 1.00 52.25 2878 CG HIS B 480 15.341 88.270 43.286 1.00 57.22 2879 ND1 HIS B 480 14.337 88.075 42.364 1.00 61.37 2880 CD2 HIS B 480 14.778 88.942 44.319 1.00 59.16 2881 CE1 HIS B 480 13.216 88.607 42.815 1.00 59.88 2882 NE2 HIS B 480 13.456 89.140 44.000 1.00 66.11 2883 N ASN B 481 17.971 91.253 42.430 1.00 56.65 2884 CA ASN B 481 18.206 92.543 43.070 1.00 59.93 2885 C ASN B 481 19.660 92.591 43.519 1.00 59.65 2886 O ASN B 481 20.571 92.569 42.695 1.00 61.04 2887 CB ASN B 481 17.288 92.751 44.282 1.00 64.65 2888 CG ASN B 481 15.852 93.022 43.890 1.00 72.38 2889 OG1 ASN B 481 15.563 93.964 43.147 1.00 74.96 2890 ND2 ASN B 481 14.938 92.199 44.393 1.00 75.60 2891 N GLU B 482 19.872 92.625 44.827 1.00 58.97 2892 CA GLU B 482 21.213 92.697 45.396 1.00 58.55 2893 C GLU B 482 21.815 91.346 45.782 1.00 55.30 2894 O GLU B 482 23.013 91.253 46.044 1.00 57.27 2895 CB GLU B 482 21.176 93.607 46.627 1.00 65.42 2896 CG GLU B 482 19.760 93.813 47.172 1.00 73.94 2897 CD GLU B 482 19.735 94.473 48.532 1.00 80.29 2898 OE1 GLU B 482 20.168 93.830 49.513 1.00 86.31 2899 OE2 GLU B 482 19.284 95.633 48.620 1.00 82.73 2900 N VAL B 483 20.997 90.301 45.814 1.00 50.25 2901 CA VAL B 483 21.487 88.988 46.211 1.00 45.78 2902 C VAL B 483 21.733 88.025 45.052 1.00 43.04 2903 O VAL B 483 20.880 87.834 44.198 1.00 41.34 2904 CB VAL B 483 20.527 88.339 47.233 1.00 43.76 2905 CG1 VAL B 483 19.129 88.283 46.668 1.00 46.25 2906 CG2 VAL B 483 21.011 86.946 47.594 1.00 41.37 2907 N GLN B 484 22.912 87.412 45.050 1.00 42.30 2908 CA GLN B 484 23.300 86.474 44.005 1.00 43.21 2909 C GLN B 484 22.658 85.091 44.141 1.00 42.48 2910 O GLN B 484 22.538 84.545 45.244 1.00 41.64 2911 CB GLN B 484 24.826 86.331 43.971 1.00 45.96 2912 CG GLN B 484 25.324 85.269 42.999 1.00 54.43 2913 CD GLN B 484 26.840 85.173 42.941 1.00 59.02 2914 OE1 GLN B 484 27.391 84.200 42.423 1.00 59.71 2915 NE2 GLN B 484 27.522 86.190 43.464 1.00 61.46 2916 N LEU B 485 22.239 84.539 43.006 1.00 38.99 2917 CA LEU B 485 21.618 83.218 42.953 1.00 39.17 2918 C LEU B 485 22.700 82.142 42.853 1.00 40.35 2919 O LEU B 485 23.822 82.417 42.430 1.00 37.39 2920 CB LEU B 485 20.705 83.107 41.725 1.00 37.16 2921 CG LEU B 485 19.579 84.140 41.602 1.00 39.66 2922 CD1 LEU B 485 18.836 83.930 40.293 1.00 39.30 2923 CD2 LEU B 485 18.644 84.020 42.795 1.00 40.56 2924 N PRO B 486 22.373 80.900 43.242 1.00 42.55 2925 CA PRO B 486 23.366 79.828 43.158 1.00 46.30 2926 C PRO B 486 23.750 79.660 41.688 1.00 49.32 2927 O PRO B 486 22.916 79.852 40.806 1.00 48.81 2928 CB PRO B 486 22.606 78.609 43.675 1.00 45.64 2929 CG PRO B 486 21.532 79.187 44.528 1.00 45.29 2930 CD PRO B 486 21.095 80.394 43.769 1.00 40.65 2931 N ASP B 487 24.997 79.290 41.429 1.00 53.39 2932 CA ASP B 487 25.465 79.093 40.062 1.00 57.75 2933 C ASP B 487 24.660 77.997 39.350 1.00 57.25 2934 O ASP B 487 24.205 78.176 38.213 1.00 57.75 2935 CB ASP B 487 26.944 78.708 40.077 1.00 67.82 2936 CG ASP B 487 27.577 78.779 38.703 1.00 76.17 2937 OD1 ASP B 487 26.945 78.309 37.734 1.00 84.77 2938 OD2 ASP B 487 28.711 79.297 38.592 1.00 86.94 2939 N ALA B 488 24.478 76.873 40.035 1.00 54.64 2940 CA ALA B 488 23.752 75.729 39.493 1.00 53.45 2941 C ALA B 488 22.421 76.069 38.837 1.00 52.74 2942 O ALA B 488 21.843 75.241 38.134 1.00 53.06 2943 CB ALA B 488 23.530 74.708 40.585 1.00 53.75 2944 N ARG B 489 21.938 77.287 39.056 1.00 50.96 2945 CA ARG B 489 20.660 77.704 38.491 1.00 47.84 2946 C ARG B 489 20.705 78.164 37.036 1.00 45.10 2947 O ARG B 489 19.681 78.158 36.363 1.00 43.37 2948 CB ARG B 489 20.046 78.808 39.354 1.00 48.99 2949 CG ARG B 489 19.232 78.294 40.524 1.00 50.01 2950 CD ARG B 489 17.761 78.427 40.227 1.00 50.36 2951 NE ARG B 489 17.187 79.581 40.905 1.00 56.65 2952 CZ ARG B 489 16.048 80.166 40.557 1.00 58.23 2953 NH1 ARG B 489 15.352 79.714 39.522 1.00 61.07 2954 NH2 ARG B 489 15.594 81.193 41.260 1.00 59.63 2955 N HIS B 490 21.872 78.573 36.551 1.00 42.41 2956 CA HIS B 490 21.965 79.024 35.166 1.00 41.63 2957 C HIS B 490 22.952 78.210 34.334 1.00 39.71 2958 O HIS B 490 23.768 77.471 34.865 1.00 41.30 2959 CB HIS B 490 22.348 80.508 35.100 1.00 42.40 2960 CG HIS B 490 23.720 80.807 35.614 1.00 43.27 2961 ND1 HIS B 490 23.966 81.177 36.919 1.00 42.27 2962 CD2 HIS B 490 24.926 80.779 34.999 1.00 44.41 2963 CE1 HIS B 490 25.262 81.364 37.086 1.00 39.88 2964 NE2 HIS B 490 25.868 81.130 35.934 1.00 45.37 2965 N SER B 491 22.858 78.355 33.020 1.00 37.20 2966 CA SER B 491 23.734 77.654 32.095 1.00 36.36 2967 C SER B 491 24.401 78.685 31.173 1.00 33.06 2968 O SER B 491 23.721 79.428 30.461 1.00 33.77 2969 CB SER B 491 22.910 76.651 31.288 1.00 35.42 2970 OG SER B 491 23.694 76.053 30.282 1.00 43.65 2971 N THR B 492 25.728 78.722 31.188 1.00 29.90 2972 CA THR B 492 26.495 79.673 30.383 1.00 29.91 2973 C THR B 492 27.322 78.977 29.287 1.00 29.20 2974 O THR B 492 27.996 77.991 29.552 1.00 30.85 2975 CB THR B 492 27.447 80.506 31.298 1.00 29.85 2976 OG1 THR B 492 26.670 81.197 32.281 1.00 35.86 2977 CG2 THR B 492 28.234 81.541 30.498 1.00 28.05 2978 N THR B 493 27.281 79.505 28.065 1.00 29.49 2979 CA THR B 493 28.032 78.913 26.957 1.00 30.19 2980 C THR B 493 29.501 79.295 27.056 1.00 32.39 2981 O THR B 493 29.863 80.210 27.786 1.00 30.70 2982 CB THR B 493 27.502 79.378 25.568 1.00 27.82 2983 OG1 THR B 493 27.592 80.806 25.460 1.00 30.48 2984 CG2 THR B 493 26.067 78.953 25.372 1.00 22.03 2985 N GLN B 494 30.347 78.586 26.322 1.00 35.09 2986 CA GLN B 494 31.779 78.879 26.330 1.00 38.19 2987 C GLN B 494 32.032 80.091 25.449 1.00 36.48 2988 O GLN B 494 31.360 80.270 24.432 1.00 35.75 2989 CB GLN B 494 32.581 77.696 25.775 1.00 43.09 2990 CG GLN B 494 32.502 76.433 26.610 1.00 58.35 2991 CD GLN B 494 32.929 76.666 28.042 1.00 65.11 2992 OE1 GLN B 494 34.003 77.209 28.303 1.00 71.67 2993 NE2 GLN B 494 32.088 76.255 28.982 1.00 71.87 2994 N PRO B 495 33.002 80.939 25.828 1.00 36.89 2995 CA PRO B 495 33.322 82.130 25.037 1.00 38.37 2996 C PRO B 495 33.609 81.737 23.587 1.00 40.80 2997 O PRO B 495 34.314 80.763 23.327 1.00 40.76 2998 CB PRO B 495 34.557 82.680 25.729 1.00 37.83 2999 CG PRO B 495 34.315 82.300 27.174 1.00 40.41 3000 CD PRO B 495 33.809 80.884 27.061 1.00 35.81 3001 N ARG B 496 33.040 82.480 22.650 1.00 42.05 3002 CA ARG B 496 33.255 82.208 21.240 1.00 47.69 3003 C ARG B 496 33.772 83.454 20.542 1.00 51.66 3004 O ARG B 496 33.283 84.558 20.784 1.00 51.95 3005 CB ARG B 496 31.954 81.751 20.584 1.00 45.81 3006 CG ARG B 496 31.599 80.317 20.892 1.00 51.53 3007 CD ARG B 496 30.217 79.947 20.391 1.00 53.72 3008 NE ARG B 496 30.175 78.554 19.963 1.00 57.50 3009 CZ ARG B 496 30.608 78.122 18.783 1.00 58.59 3010 NH1 ARG B 496 31.111 78.974 17.901 1.00 57.22 3011 NH2 ARG B 496 30.542 76.832 18.488 1.00 65.31 3012 N LYS B 497 34.773 83.281 19.687 1.00 56.98 3013 CA LYS B 497 35.335 84.408 18.953 1.00 61.91 3014 C LYS B 497 34.301 84.867 17.955 1.00 63.97 3015 O LYS B 497 33.300 84.195 17.729 1.00 64.61 3016 CB LYS B 497 36.587 84.003 18.172 1.00 66.35 3017 CG LYS B 497 37.848 83.781 18.987 1.00 74.14 3018 CD LYS B 497 38.993 83.359 18.066 1.00 80.69 3019 CE LYS B 497 40.304 83.192 18.814 1.00 84.48 3020 NZ LYS B 497 41.385 82.739 17.889 1.00 88.26 3021 N THR B 498 34.555 86.017 17.352 1.00 67.67 3022 CA THR B 498 33.669 86.572 16.342 1.00 71.26 3023 C THR B 498 34.550 87.284 15.340 1.00 73.04 3024 O THR B 498 35.743 86.990 15.236 1.00 72.83 3025 CB THR B 498 32.679 87.585 16.945 1.00 71.80 3026 OG1 THR B 498 33.392 88.555 17.721 1.00 71.58 3027 CG2 THR B 498 31.670 86.878 17.819 1.00 73.61 3028 N LYS B 499 33.962 88.220 14.605 1.00 75.57 3029 CA LYS B 499 34.705 88.993 13.620 1.00 77.62 3030 C LYS B 499 35.427 90.142 14.321 1.00 77.92 3031 O LYS B 499 34.791 91.096 14.768 1.00 79.19 3032 CB LYS B 499 33.752 89.558 12.567 1.00 80.22 3033 CG LYS B 499 33.172 88.531 11.604 1.00 81.04 3034 CD LYS B 499 34.203 88.093 10.571 1.00 83.26 3035 CE LYS B 499 33.569 87.232 9.487 1.00 84.81 3036 NZ LYS B 499 34.545 86.864 8.425 1.00 86.04 3037 N GLY B 500 36.748 90.034 14.433 1.00 76.91 3038 CA GLY B 500 37.544 91.077 15.061 1.00 75.83 3039 C GLY B 500 37.141 91.560 16.445 1.00 75.14 3040 O GLY B 500 37.971 91.576 17.355 1.00 75.52 3041 N SER B 501 35.882 91.958 16.605 1.00 73.08 3042 CA SER B 501 35.370 92.468 17.875 1.00 71.65 3043 C SER B 501 36.008 91.836 19.106 1.00 68.64 3044 O SER B 501 36.690 92.515 19.877 1.00 71.13 3045 CB SER B 501 33.854 92.279 17.953 1.00 74.43 3046 OG SER B 501 33.524 90.933 18.241 1.00 80.92 3047 N GLY B 502 35.786 90.540 19.290 1.00 63.14 3048 CA GLY B 502 36.344 89.859 20.443 1.00 54.62 3049 C GLY B 502 35.552 88.618 20.803 1.00 48.04 3050 O GLY B 502 35.469 87.683 20.006 1.00 48.08 3051 N PHE B 503 34.958 88.599 21.994 1.00 40.50 3052 CA PHE B 503 34.189 87.427 22.408 1.00 33.81 3053 C PHE B 503 32.773 87.692 22.888 1.00 28.39 3054 O PHE B 503 32.408 88.811 23.244 1.00 26.35 3055 CB PHE B 503 34.919 86.662 23.517 1.00 35.09 3056 CG PHE B 503 36.263 86.148 23.119 1.00 34.16 3057 CD1 PHE B 503 37.381 86.970 23.174 1.00 35.05 3058 CD2 PHE B 503 36.411 84.845 22.670 1.00 35.90 3059 CE1 PHE B 503 38.633 86.501 22.783 1.00 36.00 3060 CE2 PHE B 503 37.656 84.362 22.274 1.00 40.04 3061 CZ PHE B 503 38.771 85.192 22.329 1.00 38.82 3062 N PHE B 504 31.975 86.633 22.884 1.00 26.16 3063 CA PHE B 504 30.612 86.709 23.369 1.00 25.00 3064 C PHE B 504 30.286 85.418 24.096 1.00 26.57 3065 O PHE B 504 30.892 84.379 23.833 1.00 26.73 3066 CB PHE B 504 29.616 86.960 22.242 1.00 22.46 3067 CG PHE B 504 29.330 85.766 21.382 1.00 27.70 3068 CD1 PHE B 504 28.260 84.926 21.667 1.00 28.94 3069 CD2 PHE B 504 30.086 85.517 20.243 1.00 31.34 3070 CE1 PHE B 504 27.938 83.857 20.827 1.00 30.08 3071 CE2 PHE B 504 29.772 84.449 19.396 1.00 32.65 3072 CZ PHE B 504 28.691 83.621 19.697 1.00 32.80 3073 N VAL B 505 29.330 85.509 25.015 1.00 23.68 3074 CA VAL B 505 28.895 84.389 25.814 1.00 24.67 3075 C VAL B 505 27.385 84.559 26.028 1.00 23.86 3076 O VAL B 505 26.875 85.672 26.051 1.00 21.24 3077 CB VAL B 505 29.674 84.392 27.161 1.00 27.95 3078 CG1 VAL B 505 29.136 85.466 28.080 1.00 25.61 3079 CG2 VAL B 505 29.643 83.042 27.786 1.00 33.51 3080 N PHE B 506 26.664 83.454 26.141 1.00 26.20 3081 CA PHE B 506 25.218 83.514 26.346 1.00 26.10 3082 C PHE B 506 24.855 82.754 27.621 1.00 24.83 3083 O PHE B 506 25.369 81.672 27.859 1.00 25.52 3084 CB PHE B 506 24.496 82.875 25.161 1.00 28.18 3085 CG PHE B 506 23.007 82.842 25.303 1.00 35.33 3086 CD1 PHE B 506 22.245 83.980 25.080 1.00 42.56 3087 CD2 PHE B 506 22.359 81.663 25.657 1.00 40.04 3088 CE1 PHE B 506 20.854 83.940 25.208 1.00 44.70 3089 CE2 PHE B 506 20.977 81.613 25.789 1.00 40.54 3090 CZ PHE B 506 20.223 82.749 25.564 1.00 42.12 3091 N SER B 507 23.961 83.310 28.427 1.00 24.69 3092 CA SER B 507 23.550 82.659 29.674 1.00 24.73 3093 C SER B 507 22.022 82.535 29.745 1.00 26.40 3094 O SER B 507 21.308 83.487 29.491 1.00 25.99 3095 CB SER B 507 24.079 83.449 30.879 1.00 22.19 3096 OG SER B 507 23.653 82.860 32.091 1.00 30.30 3097 N ARG B 508 21.538 81.345 30.091 1.00 26.98 3098 CA ARG B 508 20.104 81.055 30.187 1.00 25.95 3099 C ARG B 508 19.689 80.749 31.637 1.00 24.97 3100 O ARG B 508 20.350 79.979 32.315 1.00 24.35 3101 CB ARG B 508 19.799 79.845 29.310 1.00 21.97 3102 CG ARG B 508 18.365 79.351 29.344 1.00 25.32 3103 CD ARG B 508 18.228 78.126 28.444 1.00 25.67 3104 NE ARG B 508 16.842 77.702 28.312 1.00 36.00 3105 CZ ARG B 508 16.243 76.843 29.128 1.00 36.06 3106 NH1 ARG B 508 16.918 76.307 30.137 1.00 34.19 3107 NH2 ARG B 508 14.967 76.538 28.943 1.00 34.70 3108 N LEU B 509 18.583 81.331 32.099 1.00 26.44 3109 CA LEU B 509 18.121 81.108 33.479 1.00 28.45 3110 C LEU B 509 16.627 80.806 33.560 1.00 28.87 3111 O LEU B 509 15.803 81.707 33.401 1.00 30.99 3112 CB LEU B 509 18.423 82.341 34.342 1.00 27.28 3113 CG LEU B 509 17.867 82.330 35.779 1.00 31.90 3114 CD1 LEU B 509 18.615 81.316 36.647 1.00 29.48 3115 CD2 LEU B 509 18.001 83.714 36.368 1.00 28.89 3116 N GLU B 510 16.277 79.546 33.812 1.00 31.92 3117 CA GLU B 510 14.872 79.152 33.911 1.00 34.67 3118 C GLU B 510 14.310 79.595 35.255 1.00 36.35 3119 O GLU B 510 14.948 79.401 36.288 1.00 34.66 3120 CB GLU B 510 14.725 77.630 33.757 1.00 41.07 3121 CG GLU B 510 15.217 77.090 32.404 1.00 54.35 3122 CD GLU B 510 14.925 75.603 32.189 1.00 58.86 3123 OE1 GLU B 510 15.236 74.789 33.087 1.00 61.22 3124 OE2 GLU B 510 14.393 75.251 31.111 1.00 61.34 3125 N VAL B 511 13.121 80.194 35.248 1.00 36.50 3126 CA VAL B 511 12.531 80.665 36.494 1.00 38.05 3127 C VAL B 511 11.084 80.230 36.692 1.00 42.41 3128 O VAL B 511 10.395 79.856 35.732 1.00 41.92 3129 CB VAL B 511 12.588 82.197 36.592 1.00 31.84 3130 CG1 VAL B 511 14.015 82.673 36.431 1.00 32.42 3131 CG2 VAL B 511 11.687 82.813 35.547 1.00 26.87 3132 N THR B 512 10.633 80.290 37.946 1.00 43.58 3133 CA THR B 512 9.269 79.903 38.292 1.00 48.37 3134 C THR B 512 8.294 80.998 37.899 1.00 50.53 3135 O THR B 512 8.706 82.113 37.584 1.00 51.77 3136 CB THR B 512 9.125 79.644 39.797 1.00 48.57 3137 OG1 THR B 512 9.460 80.834 40.519 1.00 46.96 3138 CG2 THR B 512 10.046 78.515 40.234 1.00 45.82 3139 N ARG B 513 7.002 80.678 37.912 1.00 53.29 3140 CA ARG B 513 5.971 81.648 37.556 1.00 55.54 3141 C ARG B 513 6.043 82.819 38.523 1.00 55.38 3142 O ARG B 513 5.859 83.977 38.138 1.00 55.22 3143 CB ARG B 513 4.582 81.006 37.636 1.00 59.23 3144 CG ARG B 513 3.563 81.601 36.672 1.00 65.98 3145 CD ARG B 513 3.326 83.081 36.916 1.00 74.12 3146 NE ARG B 513 2.773 83.742 35.735 1.00 80.97 3147 CZ ARG B 513 2.403 85.019 35.687 1.00 83.64 3148 NH1 ARG B 513 2.516 85.791 36.760 1.00 86.02 3149 NH2 ARG B 513 1.927 85.528 34.557 1.00 85.44 3150 N ALA B 514 6.315 82.501 39.783 1.00 55.03 3151 CA ALA B 514 6.414 83.504 40.832 1.00 55.46 3152 C ALA B 514 7.496 84.539 40.529 1.00 56.10 3153 O ALA B 514 7.210 85.734 40.426 1.00 56.61 3154 CB ALA B 514 6.692 82.825 42.173 1.00 54.05 3155 N GLU B 515 8.741 84.091 40.388 1.00 55.46 3156 CA GLU B 515 9.819 85.025 40.105 1.00 55.34 3157 C GLU B 515 9.649 85.651 38.729 1.00 54.83 3158 O GLU B 515 10.190 86.723 38.456 1.00 52.33 3159 CB GLU B 515 11.187 84.335 40.232 1.00 57.76 3160 CG GLU B 515 11.221 82.884 39.788 1.00 62.58 3161 CD GLU B 515 12.518 82.184 40.163 1.00 63.27 3162 OE1 GLU B 515 13.035 82.432 41.271 1.00 64.89 3163 OE2 GLU B 515 13.014 81.372 39.359 1.00 66.59 3164 N THR B 516 8.884 84.992 37.866 1.00 55.79 3165 CA THR B 516 8.644 85.528 36.534 1.00 57.81 3166 C THR B 516 7.778 86.782 36.636 1.00 58.51 3167 O THR B 516 7.778 87.612 35.726 1.00 57.71 3168 CB THR B 516 7.951 84.499 35.634 1.00 61.48 3169 CG THR B 516 8.056 84.862 34.187 1.00 66.54 3170 CD1 THR B 516 9.172 84.777 33.403 1.00 67.26 3171 CD2 THR B 516 7.039 85.460 33.375 1.00 69.56 3172 NE1 THR B 516 8.915 85.291 32.154 1.00 71.76 3173 CE2 THR B 516 7.613 85.718 32.110 1.00 70.88 3174 CE3 THR B 516 5.700 85.807 33.593 1.00 70.94 3175 CZ2 THR B 516 6.894 86.308 31.066 1.00 73.50 3176 CZ3 THR B 516 4.982 86.396 32.552 1.00 74.37 3177 CH2 THR B 516 5.584 86.639 31.304 1.00 74.71 3178 N GLU B 517 7.047 86.918 37.744 1.00 59.66 3179 CA GLU B 517 6.191 88.085 37.972 1.00 61.72 3180 C GLU B 517 7.035 89.299 38.354 1.00 59.87 3181 O GLU B 517 6.606 90.441 38.196 1.00 58.60 3182 CB GLU B 517 5.182 87.818 39.097 1.00 68.82 3183 CG GLU B 517 4.284 86.612 38.879 1.00 80.60 3184 CD GLU B 517 3.242 86.452 39.976 1.00 87.42 3185 OE1 GLU B 517 3.369 87.128 41.021 1.00 94.80 3186 OE2 GLU B 517 2.301 85.645 39.800 1.00 95.35 3187 N GLU B 518 8.234 89.045 38.867 1.00 57.92 3188 CA GLU B 518 9.132 90.120 39.264 1.00 55.74 3189 C GLU B 518 10.416 90.057 38.436 1.00 54.32 3190 O GLU B 518 11.498 90.393 38.924 1.00 52.85 3191 CB GLU B 518 9.454 90.000 40.745 1.00 54.10 3192 N LYS B 519 10.287 89.646 37.176 1.00 52.69 3193 CA LYS B 519 11.448 89.518 36.309 1.00 52.35 3194 C LYS B 519 12.206 90.819 36.159 1.00 51.69 3195 O LYS B 519 13.397 90.822 35.854 1.00 49.61 3196 CB LYS B 519 11.039 88.983 34.937 1.00 54.31 3197 CG LYS B 519 10.205 89.912 34.088 1.00 55.80 3198 CD LYS B 519 9.723 89.162 32.859 1.00 60.32 3199 CE LYS B 519 8.794 90.002 32.011 1.00 64.05 3200 NZ LYS B 519 8.223 89.191 30.898 1.00 70.92 3201 N ASP B 520 11.511 91.924 36.388 1.00 52.66 3202 CA ASP B 520 12.105 93.251 36.288 1.00 54.22 3203 C ASP B 520 13.209 93.396 37.336 1.00 53.07 3204 O ASP B 520 14.075 94.264 37.229 1.00 52.75 3205 CE ASP B 520 11.032 94.311 36.537 1.00 61.14 3206 CG ASP B 520 9.620 93.779 36.308 1.00 71.19 3207 OD1 ASP B 520 9.300 93.407 35.155 1.00 76.53 3208 OD2 ASP B 520 8.834 93.729 37.283 1.00 72.86 3209 N GLU B 521 13.177 92.533 38.343 1.00 51.01 3210 CA GLU B 521 14.157 92.582 39.416 1.00 50.49 3211 C GLU B 521 15.394 91.714 39.201 1.00 47.73 3212 O GLU B 521 16.372 91.838 39.935 1.00 48.58 3213 CB GLU B 521 13.493 92.200 40.738 1.00 53.54 3214 CG GLU B 521 12.427 93.177 41.199 1.00 60.11 3215 CD GLU B 521 11.705 92.699 42.442 1.00 65.41 3216 OE1 GLU B 521 12.361 92.497 43.486 1.00 67.98 3217 OE2 GLU B 521 10.471 92.521 42.374 1.00 73.58 3218 N PHE B 522 15.359 90.828 38.213 1.00 42.66 3219 CA PHE B 522 16.519 89.985 37.963 1.00 38.90 3220 C PHE B 522 17.583 90.753 37.208 1.00 35.93 3221 O PHE B 522 17.276 91.579 36.345 1.00 38.85 3222 CB PHE B 522 16.122 88.716 37.214 1.00 36.56 3223 CG PHE B 522 15.419 87.710 38.081 1.00 39.04 3224 CD1 PHE B 522 14.106 87.927 38.495 1.00 42.28 3225 CD2 PHE B 522 16.087 86.574 38.539 1.00 36.78 3226 CE1 PHE B 522 13.468 87.029 39.362 1.00 44.30 3227 CE2 PHE B 522 15.461 85.673 39.405 1.00 40.92 3228 CZ PHE B 522 14.146 85.901 39.817 1.00 39.51 3229 N ILE B 523 18.837 90.492 37.555 1.00 31.27 3230 CA ILE B 523 19.959 91.173 36.944 1.00 29.65 3231 C ILE B 523 21.049 90.211 36.483 1.00 29.13 3232 O ILE B 523 21.360 89.236 37.164 1.00 27.36 3233 CB ILE B 523 20.567 92.180 37.937 1.00 34.21 3234 CG1 ILE B 523 19.528 93.251 38.282 1.00 37.38 3235 CG2 ILE B 523 21.827 92.796 37.364 1.00 34.94 3236 CD1 ILE B 523 19.981 94.227 39.354 1.00 38.56 3237 N CYS B 524 21.610 90.498 35.311 1.00 26.34 3238 CA CYS B 524 22.686 89.699 34.739 1.00 27.10 3239 C CYS B 524 23.946 90.500 34.962 1.00 26.67 3240 O CYS B 524 24.010 91.655 34.569 1.00 27.58 3241 CB CYS B 524 22.473 89.497 33.226 1.00 24.27 3242 SG CYS B 524 23.823 88.626 32.363 1.00 37.60 3243 N ARG B 525 24.951 89.886 35.572 1.00 26.37 3244 CA ARG B 525 26.194 90.576 35.856 1.00 26.35 3245 C ARG B 525 27.419 89.887 35.304 1.00 26.72 3246 O ARG B 525 27.561 88.671 35.400 1.00 29.04 3247 CB ARG B 525 26.376 90.748 37.361 1.00 29.81 3248 CG ARG B 525 27.713 91.393 37.728 1.00 35.40 3249 CD ARG B 525 27.652 92.058 39.099 1.00 46.51 3250 NE ARG B 525 27.796 91.113 40.193 1.00 50.77 3251 CZ ARG B 525 27.461 91.379 41.451 1.00 55.09 3252 NH1 ARG B 525 26.951 92.565 41.763 1.00 54.58 3253 NH2 ARG B 525 27.650 90.464 42.397 1.00 56.77 3254 N ALA B 526 28.311 90.680 34.731 1.00 25.38 3255 CA ALA B 526 29.528 90.142 34.180 1.00 25.38 3256 C ALA B 526 30.721 90.728 34.925 1.00 25.99 3257 O ALA B 526 30.751 91.933 35.210 1.00 25.50 3258 CB ALA B 526 29.629 90.484 32.696 1.00 25.98 3259 N VAL B 527 31.684 89.872 35.259 1.00 23.84 3260 CA VAL B 527 32.895 90.333 35.902 1.00 25.15 3261 C VAL B 527 33.972 90.078 34.880 1.00 26.30 3262 O VAL B 527 34.119 88.958 34.394 1.00 26.20 3263 CB VAL B 527 33.235 89.557 37.177 1.00 24.43 3264 CG1 VAL B 527 34.588 89.990 37.661 1.00 26.95 3265 CG2 VAL B 527 32.191 89.819 38.251 1.00 28.13 3266 N HIS B 528 34.738 91.115 34.569 1.00 26.24 3267 CA HIS B 528 35.772 91.018 33.564 1.00 29.14 3268 C HIS B 528 36.822 92.102 33.805 1.00 31.86 3269 O HIS B 528 36.509 93.216 34.239 1.00 31.05 3270 CB HIS B 528 35.121 91.172 32.179 1.00 29.03 3271 CG HIS B 528 36.077 91.082 31.035 1.00 29.34 3272 ND1 HIS B 528 36.934 92.109 30.696 1.00 33.33 3273 CD2 HIS B 528 36.317 90.090 30.144 1.00 28.93 3274 CE1 HIS B 528 37.655 91.755 29.651 1.00 26.07 3275 NE2 HIS B 528 37.302 90.530 29.295 1.00 32.19 3276 N GLU B 529 38.064 91.757 33.501 1.00 34.08 3277 CA GLU B 529 39.207 92.636 33.676 1.00 39.76 3278 C GLU B 529 39.110 94.037 33.066 1.00 41.50 3279 O GLU B 529 39.410 95.020 33.740 1.00 41.48 3280 CB GLU B 529 40.462 91.959 33.122 1.00 43.03 3281 CG GLU B 529 41.665 92.898 33.086 1.00 56.19 3282 CD GLU B 529 42.827 92.361 32.274 1.00 62.66 3283 OE1 GLU B 529 43.812 93.111 32.093 1.00 63.52 3284 OE2 GLU B 529 42.758 91.198 31.819 1.00 65.43 3285 N ALA B 530 38.703 94.121 31.800 1.00 42.51 3286 CA ALA B 530 38.622 95.399 31.094 1.00 46.03 3287 C ALA B 530 37.495 96.331 31.504 1.00 49.29 3288 O ALA B 530 37.447 97.476 31.056 1.00 50.87 3289 CB ALA B 530 38.557 95.157 29.587 1.00 39.71 3290 N ALA B 531 36.595 95.849 32.352 1.00 52.89 3291 CA ALA B 531 35.467 96.651 32.798 1.00 56.14 3292 C ALA B 531 35.801 97.570 33.976 1.00 59.66 3293 O ALA B 531 35.357 97.342 35.096 1.00 61.00 3294 CB ALA B 531 34.305 95.736 33.162 1.00 52.83 3295 N SER B 532 36.588 98.608 33.730 1.00 63.07 3296 CA SER B 532 36.927 99.544 34.795 1.00 66.03 3297 C SER B 532 35.822 100.594 34.850 1.00 66.08 3298 O SER B 532 35.317 101.031 33.814 1.00 65.35 3299 CB SER B 532 38.270 100.216 34.507 1.00 68.98 3300 OG SER B 532 38.184 101.074 33.384 1.00 74.64 3301 N PRO B 533 35.427 101.019 36.057 1.00 66.51 3302 CA PRO B 533 35.887 100.669 37.404 1.00 65.99 3303 C PRO B 533 35.374 99.349 37.983 1.00 63.48 3304 O PRO B 533 34.327 98.840 37.582 1.00 64.33 3305 CB PRO B 533 35.397 101.843 38.227 1.00 69.06 3306 CG PRO B 533 34.044 102.061 37.629 1.00 71.08 3307 CD PRO B 533 34.358 102.030 36.137 1.00 70.23 3308 N SER B 534 36.134 98.817 38.935 1.00 59.21 3309 CA SER B 534 35.796 97.591 39.648 1.00 55.01 3310 C SER B 534 35.452 96.326 38.852 1.00 50.27 3311 O SER B 534 34.725 95.470 39.347 1.00 48.58 3312 CB SER B 534 34.666 97.894 40.625 1.00 58.20 3313 OG SER B 534 33.587 98.526 39.962 1.00 63.36 3314 N GLN B 535 35.984 96.213 37.639 1.00 44.89 3315 CA GLN B 535 35.771 95.057 36.770 1.00 42.88 3316 C GLN B 535 34.395 94.406 36.823 1.00 41.55 3317 O GLN B 535 34.279 93.181 36.806 1.00 40.80 3318 CB GLN B 535 36.831 93.967 37.020 1.00 37.08 3319 CG GLN B 535 37.869 94.298 38.044 1.00 47.40 3320 CD GLN B 535 38.684 95.499 37.669 1.00 44.36 3321 OE1 GLN B 535 38.862 96.407 38.475 1.00 47.59 3322 NE2 GLN B 535 39.185 95.521 36.436 1.00 54.70 3323 N THR B 536 33.348 95.213 36.874 1.00 39.97 3324 CA THR B 536 32.012 94.650 36.893 1.00 40.62 3325 C THR B 536 31.025 95.487 36.077 1.00 37.57 3326 O THR B 536 31.042 96.707 36.125 1.00 40.85 3327 CB THR B 536 31.508 94.463 38.353 1.00 42.38 3328 OG1 THR B 536 30.112 94.142 38.337 1.00 44.59 3329 CG2 THR B 536 31.730 95.719 39.168 1.00 49.65 3330 N VAL B 537 30.190 94.812 35.299 1.00 35.29 3331 CA VAL B 537 29.182 95.453 34.468 1.00 31.25 3332 C VAL B 537 27.922 94.604 34.563 1.00 29.01 3333 O VAL B 537 27.985 93.382 34.401 1.00 30.11 3334 CB VAL B 537 29.604 95.494 32.983 1.00 34.80 3335 CG1 VAL B 537 28.516 96.148 32.161 1.00 35.52 3336 CG2 VAL B 537 30.888 96.259 32.822 1.00 37.19 3337 N GLN B 538 26.780 95.235 34.808 1.00 26.73 3338 CA GLN B 538 25.533 94.493 34.933 1.00 26.74 3339 C GLN B 538 24.329 95.224 34.368 1.00 27.53 3340 O GLN B 538 24.351 96.431 34.198 1.00 29.89 3341 CB GLN B 538 25.265 94.176 36.400 1.00 28.48 3342 CG GLN B 538 24.976 95.392 37.266 1.00 25.88 3343 CD GLN B 538 24.747 95.005 38.722 1.00 28.51 3344 OE1 GLN B 538 25.498 94.210 39.290 1.00 31.66 3345 NE2 GLN B 538 23.715 95.565 39.328 1.00 27.39 3346 N ARG B 539 23.266 94.487 34.087 1.00 28.05 3347 CA ARG B 539 22.070 95.107 33.565 1.00 30.72 3348 C ARG B 539 20.858 94.312 33.986 1.00 31.33 3349 O ARG B 539 20.897 93.083 34.023 1.00 32.42 3350 CB ARG B 539 22.137 95.180 32.039 1.00 36.30 3351 CG ARG B 539 21.124 96.112 31.414 1.00 45.60 3352 CD ARG B 539 21.771 96.859 30.270 1.00 57.97 3353 NE ARG B 539 23.009 97.482 30.729 1.00 69.46 3354 CZ ARG B 539 23.855 98.147 29.950 1.00 78.18 3355 NH1 ARG B 539 23.604 98.284 28.653 1.00 83.01 3356 NH2 ARG B 539 24.959 98.673 30.470 1.00 81.89 3357 N ALA B 540 19.782 95.022 34.301 1.00 31.92 3358 CA ALA B 540 18.546 94.393 34.717 1.00 34.50 3359 C ALA B 540 17.826 93.909 33.466 1.00 36.68 3360 O ALA B 540 18.068 94.410 32.361 1.00 34.62 3361 CB ALA B 540 17.693 95.391 35.479 1.00 33.91 3362 N VAL B 541 16.974 92.906 33.640 1.00 39.73 3363 CA VAL B 541 16.214 92.346 32.528 1.00 44.47 3364 C VAL B 541 15.351 93.436 31.882 1.00 46.91 3365 O VAL B 541 14.476 94.005 32.527 1.00 44.53 3366 CB VAL B 541 15.305 91.185 33.010 1.00 42.49 3367 CG1 VAL B 541 14.242 90.885 31.970 1.00 47.96 3368 CG2 VAL B 541 16.140 89.945 33.269 1.00 42.43 3369 N SER B 542 15.603 93.731 30.611 1.00 52.25 3370 CA SER B 542 14.829 94.760 29.926 1.00 60.05 3371 C SER B 542 13.426 94.226 29.679 1.00 64.25 3372 O SER B 542 13.247 93.050 29.357 1.00 65.22 3373 CB SER B 542 15.490 95.157 28.600 1.00 60.43 3374 OG SER B 542 15.524 94.070 27.696 1.00 65.30 3375 N VAL B 543 12.432 95.090 29.844 1.00 68.19 3376 CA VAL B 543 11.043 94.694 29.656 1.00 72.45 3377 C VAL B 543 10.277 95.772 28.898 1.00 74.32 3378 O VAL B 543 9.621 96.630 29.497 1.00 75.99 3379 CB VAL B 543 10.353 94.452 31.016 1.00 74.41 3380 CG1 VAL B 543 8.895 94.070 30.801 1.00 76.37 3381 CG2 VAL B 543 11.086 93.367 31.782 1.00 75.78 3382 O HOH B 1 28.242 81.091 34.909 1.00 54.75 3383 O HOH B 2 20.156 98.063 34.554 1.00 37.27 3384 O HOH B 3 9.164 79.181 26.395 1.00 46.90 3385 O HOH B 4 40.362 78.148 37.537 1.00 44.93 3386 O HOH B 5 26.513 97.015 29.107 1.00 46.77 3387 O HON B 6 24.671 83.376 40.011 1.00 40.32 3388 O HOH B 7 50.797 88.328 45.010 1.00 50.21 3389 O HOH B 8 30.596 75.260 16.415 1.00 61.75 3390 O HOH B 9 39.623 81.063 40.390 1.00 39.17 3391 O HOH B 10 10.819 88.759 44.203 1.00 64.36 3392 O HOH B 11 43.896 82.650 46.479 1.00 45.74 3393 O HOH B 12 40.405 77.131 40.006 1.00 39.34 3394 O HOH B 13 28.630 51.829 41.383 1.00 56.15 3395 O HOH B 14 18.197 77.472 34.045 1.00 46.48 3396 O HOH B 15 29.246 81.729 23.290 1.00 36.55 3397 O HOH B 16 27.005 76.944 32.905 1.00 48.95 3398 O HOH B 17 46.365 79.161 30.402 1.00 50.90 3399 O HOH B 18 29.027 56.778 36.404 1.00 58.83 3400 O HOH B 19 32.617 59.584 31.846 1.00 61.24 3401 O HOH B 20 46.447 87.589 46.492 1.00 58.37 3402 O HOH B 21 37.888 95.014 40.873 1.00 57.48 3403 O HOH B 22 55.424 66.383 26.960 1.00 60.62 3404 O HOH B 23 49.953 85.610 35.164 1.00 49.14 3405 O HOH B 24 0.662 87.508 40.326 1.00 63.67 3406 O HOH B 25 19.011 94.187 29.591 1.00 40.50 3407 O HOH B 26 43.242 49.660 46.237 1.00 58.12 3408 O HOH B 27 40.629 78.744 31.911 1.00 52.34 3409 O HOH B 28 40.803 72.686 34.647 1.00 52.41 3410 O HOH B 29 1.434 81.662 24.774 1.00 63.47 3411 O HOH B 30 29.558 77.458 32.128 1.00 56.91 3412 O HOH B 31 40.590 70.716 43.907 1.00 49.06 3413 O HOH B 32 23.070 95.434 42.368 1.00 59.31 3414 O HOH B 33 58.388 76.819 41.695 1.00 51.40 3415 O HOH B 34 50.954 79.227 44.916 1.00 49.71 3416 O HOH B 35 34.068 54.729 35.446 1.00 64.98 3417 O HOH B 36 29.928 90.630 44.684 1.00 55.97 3418 O HOH B 37 29.718 98.417 28.749 1.00 56.10 3419 O HOH B 38 34.139 96.711 23.956 1.00 48.69 3420 O HOH B 39 38.006 89.010 17.278 1.00 58.57 3421 O HOH B 40 52.915 67.142 28.195 1.00 54.81 3422 O HOH B 41 41.555 51.194 38.581 1.00 65.02 3423 O HOH B 42 52.498 94.849 41.604 1.00 60.95 3424 O HOH B 43 23.412 53.599 37.661 1.00 59.29 3425 O HOH B 44 28.241 88.615 44.746 1.00 64.70 3426 O HOH B 45 54.871 85.305 45.726 1.00 57.91 3427 O HOH B 46 9.818 81.648 43.286 1.00 54.20 3428 O HOH B 47 26.359 91.470 45.088 1.00 59.40 3429 O HOH B 48 28.072 63.227 38.869 1.00 61.07 3430 O HOH B 49 45.277 55.789 32.757 1.00 62.77 3431 O HOH B 50 44.758 73.013 29.503 1.00 54.90 3432 O HOH B 51 38.266 78.900 44.091 1.00 59.03 3433 O HOH B 52 8.212 78.463 34.558 1.00 57.55 3434 O HOH B 53 1.381 85.874 28.805 1.00 55.02 3435 O HOH B 54 26.806 78.029 35.293 1.00 62.62 3436 O HOH B 55 12.447 95.162 25.458 1.00 64.18 3437 O HOH B 56 3.811 85.411 25.179 1.00 57.80 3438 O HOH B 57 29.871 60.364 33.052 1.00 68.28 3439 O HOH B 58 19.470 76.874 31.345 1.00 42.77 3440 O HOH B 59 43.684 89.839 24.236 1.00 49.12 3441 O HOH B 60 8.499 86.927 28.688 1.00 60.00 3442 O HOH B 61 42.759 54.014 38.123 1.00 66.82 3443 O HOH B 62 57.282 92.935 37.270 1.00 61.58 3444 O HOH B 63 35.759 94.606 20.953 1.00 54.56 3445 O HOH B 64 55.504 71.596 38.010 1.00 52.20 3446 O HOH B 65 51.524 82.672 43.463 1.00 63.55 3447 O HOH B 66 25.162 92.476 24.637 1.00 49.41 3448 O HOH B 67 20.866 91.104 50.882 1.00 59.74 3449 O HOH B 68 21.567 72.397 38.063 1.00 61.59 3450 O HOH B 69 34.917 80.449 18.554 1.00 58.32 3451 O HOH B 70 58.059 62.072 40.018 1.00 67.46 3452 O HOH B 71 46.678 76.624 50.973 1.00 56.29 3453 O HOH B 72 47.970 66.515 43.658 1.00 57.89 3454 O HOH B 73 58.976 70.892 35.943 1.00 61.84 3455 O HOH B 74 37.925 102.300 36.267 1.00 70.53 3456 O HOH B 75 35.095 82.009 30.623 1.00 53.22 3457 O HOH B 76 48.950 89.607 45.995 1.00 60.73 3458 O HOH B 77 51.049 54.014 41.456 1.00 64.35 3459 O HOH B 78 9.614 90.974 28.382 1.00 59.27 3460 O HOH B 79 30.892 81.866 34.924 1.00 53.70 3461 O HOH B 80 8.623 88.500 43.305 1.00 60.32 3462 O HOH B 81 37.845 96.067 20.364 1.00 56.40 3463 O HOH B 82 38.754 86.712 18.621 1.00 62.11 3464 O HOH B 83 33.854 61.761 30.984 1.00 57.66 3465 O HOH B 84 31.092 97.083 24.789 1.00 61.70 3466 O HOH B 85 55.604 63.730 25.209 1.00 61.38 3467 O HOH B 86 10.681 91.038 44.382 1.00 67.86 3468 O HOH B 87 8.631 76.809 27.264 1.00 61.99 3469 O HOH B 88 27.366 82.163 39.549 1.00 54.45 3470 O HOH B 89 25.286 75.986 42.777 1.00 57.86 3471 O HOH B 90 37.707 77.054 41.662 1.00 58.43 3472 O HOH B 91 32.692 58.560 34.055 1.00 67.78 3473 O HOH B 92 53.944 63.193 28.977 1.00 65.22 3474 O HOH B 93 39.865 81.851 49.172 1.00 60.31 3475 O HOH B 94 31.308 61.582 30.906 1.00 61.54 3476 O HOH B 95 59.514 93.999 36.788 1.00 67.64 3477 O HOH B 96 39.447 99.425 29.592 1.00 56.59 3478 O HOH B 97 58.449 74.096 43.103 1.00 64.62 3479 O HOH B 98 29.674 63.288 40.778 1.00 66.03 3480 O HOH B 99 48.458 74.578 28.945 1.00 62.65 3481 O HOH B 100 1.217 87.605 43.348 1.00 63.95 3482 O HOH B 101 18.899 94.884 51.591 1.00 63.86 3483 O HOH B 102 32.969 77.837 30.721 1.00 62.58 3484 O HOH B 103 0.563 90.219 39.830 1.00 58.40 3485 O HOH B 104 26.801 57.949 31.582 1.00 61.34 3486 O HOH B 105 11.041 70.673 37.151 1.00 65.87 3487 O HOH B 106 22.839 96.513 26.321 1.00 61.27 3488 O HOH B 107 51.734 82.918 46.361 1.00 67.17 3489 O HOH B 108 47.037 68.251 48.363 1.00 54.90 3490 O HOH B 109 7.726 80.618 44.317 1.00 66.23 3491 O HOH B 110 32.588 73.719 18.127 1.00 59.96 3492 O HOH B 111 44.611 57.647 45.310 1.00 64.92 3493 O HOH B 112 32.288 63.471 36.999 1.00 65.68 3494 O HOH B 113 47.059 68.725 45.458 1.00 61.47 3495 O HOH B 114 52.648 70.274 44.235 1.00 60.20 3496 O HOH B 115 28.226 99.464 26.888 1.00 59.29 3497 O HOH B 116 10.671 79.859 28.221 1.00 53.05 3498 O HOH B 117 47.224 51.238 37.567 1.00 69.15 3499 O HOH B 118 2.077 82.274 29.937 1.00 62.28 3500 O HOH B 119 21.625 99.622 31.504 1.00 59.61 3501 O HOH B 120 51.285 72.528 46.379 1.00 61.94 3502 O HOH B 121 60.228 68.403 35.257 1.00 64.45 3503 O HOH B 122 40.261 93.766 43.138 1.00 63.01 3504 O HOH B 123 25.735 89.468 46.487 1.00 59.29 3505 O HOH B 124 31.385 92.796 46.304 1.00 61.69 3506 O HOH B 125 33.401 99.434 35.006 1.00 69.10 3507 O HOH B 126 53.684 58.928 43.989 1.00 61.79 3508 O HOH B 127 48.916 83.660 48.343 1.00 63.74 3509 O HOH B 128 32.974 85.797 6.578 1.00 67.04 3510 O HOH B 129 2.491 77.598 35.303 1.00 62.20 3511 O HOH B 130 39.071 89.336 19.546 1.00 66.48 3512 O HOH B 131 33.906 66.916 41.602 1.00 70.79 3513 O HOH B 132 7.009 74.725 27.690 1.00 72.41 3514 O HOH B 133 41.213 85.156 25.009 1.00 62.09 3515 O HOH B 134 53.407 88.641 45.536 1.00 61.32 3516 O HOH B 135 61.105 61.893 39.131 1.00 68.49 3517 O HOH B 136 54.402 78.303 50.147 1.00 69.04 3518 O HOH B 137 58.078 60.598 38.009 1.00 63.49 3519 O HOH B 138 23.599 84.930 47.731 1.00 53.37 3520 O HOH B 139 5.249 86.853 27.014 1.00 59.07 3521 O HOH B 140 58.796 62.599 31.318 1.00 65.35 3522 O HOH B 141 50.703 49.006 36.896 1.00 67.74 3523 O HOH B 142 11.022 88.620 46.640 1.00 67.40 3524 O HOH B 143 37.589 71.107 41.445 1.00 64.43 3525 O HOH B 144 17.187 98.039 48.494 1.00 67.27 3526 O HOH B 145 30.164 50.230 40.408 1.00 70.07

[0043] As used herein, an atomic coordinate, also referred to herein as a structure coordinate or coordinate, is a mathematical coordinate derived from mathematical equations related to the patterns obtained on diffraction of X-rays by the atoms of a protein or complex crystal. The diffraction data are typically used to calculate an electron density map, which is used to establish the positions of the individual atoms within the unit cell of the crystal. A model that substantially represents the atomic coordinates specified in Table 1, Table 2 or Table 3 includes not only models that literally represent the coordinates but also models representing a coordinate transformation of such atomic coordinates, for example, by changing the spatial orientation of the coordinates.

[0044] The present invention also includes a 3-D model that is a modification of a 3-D model that substantially represents the atomic coordinates specified in Table 1, Table 2 or Table 3. As used herein, a modification, also referred to herein as a model modification, is a model that represents an antibody Fc region that binds to a Fc receptor protein. A model modification includes, but is not limited to: a refinement of the model that substantially represents the atomic coordinates specified in Table 1, Table 2 or Table 3; a model representing any FcR-binding fragment of an antibody having the atomic coordinates specified in Table 1, Table 2 or Table 3; a model based on other Fc-Cε3/Cε4 crystals, such as a model based on a crystal disclosed in the Examples; a model produced using homology modeling techniques to, for example, incorporate all or any part of the amino acid sequence of another Fc region into a 3-D model substantially representing the atomic coordinates specified in Table 1, Table 2 or Table 3 or incorporate all or any part of the amino acid sequence of a Fc-Cε3/Cε4 into a 3-D model of another antibody; and a modification representing a Fc region that has an altered function, which preferably can be used to design a mutein with an improved function compared to an unmodified protein. As used herein, the term unmodified protein refers to a protein that has not been intentionally subjected to either random or site-directed (i.e., targeted) mutagenesis. While not being bound by theory, it is believed that the flexibility of the Cε3 and Cε4 chains of the Fc region of IgE which allows the formation of open (receptor-bound) and closed conformations, can also lead to other dynamic conformations, all of which are included in the present invention. Such flexibility is also a target for identification of development of compounds to inhibit binding of IgE to its receptor. In one embodiment, the distance between two Cε3 domains of a Fc region of the present invention ranges from about 10 angstroms to about 25 angstroms. In another embodiment, the distance between two Cε3 domains of a Fc region of the present invention ranges from about 20 angstroms to about 40 angstroms, with a range of from about 20 to about 30 angstroms being preferred.

[0045] A model of the present invention can be represented in a variety of forms including, but not limited to, listing the coordinates of all atoms comprising the model, providing a physical 3-D model, imaging the model on a computer screen, providing a picture of said model, and deriving a set of coordinates based of a picture of the model, for example by extracting coordinates from a picture or placing a similar immunoglobulin domain into the 3-D model of a human Fc-Cε3/Cε4₂₂₂ protein having SEQ ID NO:2 and deriving a model of the similar domain. Physical 3-D models are tangible and include, but are not limited to, stick models and space-filling models. The phrase “imaging the model on a computer screen” refers to the ability to express (or represent) and manipulate the model on a computer screen using appropriate computer hardware and software technology known to those skilled in the art. Such technology is available from a variety of sources including, for example, Evans and Sutherland, Salt Lake City, Utah, Biosym Technologies, San Diego, Calif., Tripos, Inc., and Molecular Simulations Inc. The phrase “providing a picture of the model” refers to the ability to generate a “hard copy” of the model. Hard copies include both motion and still pictures. Computer screen images and pictures of the model can be visualized in a number of formats including, but not limited to, electron density maps, ribbon diagrams, space-filling representations, a carbon traces, topology diagrams, lists of interatomic vectors, phi/psi/chi angle representations of the coordinates, and contact maps, examples of some of which are in the Figs. Representations of the model can include the entire model or portions thereof. A model can also be represented in a database.

[0046] A model of the present invention also defines the space surrounding that model. Such a space can be represented as a mold, or alpha-space, that can be used to predict the shape of a compound that inhibits the binding of a FcR and antibody.

[0047] In one embodiment, a model of the present invention identifies the solvent accessibility of amino acid residues of the corresponding proteins in the complex. The solvent accessibilities of the amino acids in PhFc-Cε3/Cε4₁₋₂₂₂ are indicated in Table 4. TABLE 4 IgE-Fc Residue Exposure Surface plot for: structure file = 7_more_easy.mtf coordinate set = 7_more_easy.pdb average accessible area segid resid resname residue mainchain sidechain A 336 VAL 11.0355 10.7157 11.4619 A 337 SER 6.6644 0.9102 18.1728 A 338 ALA 1.5503 1.9379 0.0000 A 339 TYR 8.1765 1.1049 11.7123 A 340 LEU 3.6795 7.1662 0.1928 A 341 SER 10.1371 1.1968 28.0177 A 342 ARG 6.2194 3.9259 7.5300 A 343 PRO 1.0168 1.4058 0.4982 A 344 SER 7.7961 2.0652 19.2580 A 345 PRO 1.3218 0.0070 3.0748 A 346 PHE 4.9773 0.0000 7.8215 A 347 ASP 3.9717 0.0000 7.9435 A 348 LEU 2.0606 0.7880 3.3332 A 349 PHE 4.1860 4.1923 4.1824 A 350 ILE 8.0920 2.3463 13.8377 A 351 ARG 12.2182 6.3068 15.5962 A 352 LYS 15.4391 4.6705 24.0540 A 353 SER 8.3827 1.7463 21.6553 A 354 PRO 0.3971 0.3072 0.5168 A 355 THR 5.7285 1.2045 11.7605 A 356 ILE 0.1440 0.2879 0.0000 A 357 THR 5.3215 0.3410 11.9621 A 358 CYS 0.0000 0.0000 0.0000 A 359 LEU 3.5251 0.0000 7.0503 A 360 VAL 0.5274 0.0632 1.1465 A 361 VAL 3.5236 0.1093 8.0760 A 362 ASP 1.8760 0.2987 3.4534 A 363 ALA 20.1207 10.3102 59.3628 A 364 ALA 15.4855 4.7737 58.3324 A 365 PRO 8.8456 4.2563 14.9647 A 366 ALA 19.4281 10.6196 54.6617 A 367 LYS 14.1954 9.3656 18.0592 A 368 GLY 19.0191 19.0191 0.0000 A 369 ALA 13.5479 3.8042 52.5228 A 370 VAL 1.9022 0.2211 4.1436 A 371 ASN 9.8425 0.1360 19.5491 A 372 LEU 3.3729 6.1984 0.5473 A 373 THR 11.0885 1.1749 24.3065 A 374 TRP 1.6039 3.8874 0.6904 A 375 SER 8.4426 0.6753 23.9772 A 376 ARG 3.0964 1.9387 3.7580 A 377 ALA 15.7221 11.6308 32.0872 A 378 SER 11.3325 9.7475 14.5025 A 379 GLY 16.4108 16.4108 0.0000 A 380 LYS 13.6283 1.9326 22.9849 A 381 PRO 15.4265 3.6481 31.1310 A 382 VAL 7.3416 6.0250 9.0971 A 383 ASN 11.3782 3.3857 19.3706 A 384 HIS 17.2932 3.2244 26.6723 A 385 SER 9.0295 7.7970 11.4946 A 386 THR 10.4147 0.8671 23.1449 A 387 ARG 8.9842 6.7673 10.2510 A 388 LYS 13.1006 1.8914 22.0680 A 389 GLU 12.0438 8.6316 14.7736 A 390 ALA 12.8310 2.6317 53.6284 A 391 ALA 26.6304 21.5969 46.7642 A 397 LEU 7.6007 6.7288 8.4727 A 398 THR 5.6519 0.0606 13.1069 A 399 VAL 0.3919 0.0000 0.9144 A 400 THR 3.3881 0.0000 7.9056 A 401 SER 0.6660 0.0000 1.9979 A 402 THR 3.4801 0.2334 7.8090 A 403 LEU 0.1292 0.0003 0.2581 A 404 PRO 8.0051 0.8129 17.5947 A 405 VAL 1.7566 3.0741 0.0000 A 406 GLY 7.5226 7.5226 0.0000 A 407 THR 7.4670 1.2753 15.7226 A 408 ALA 11.6207 1.1130 53.6516 A 409 ASP 7.3957 0.7299 14.0615 A 410 TRP 0.6616 0.0000 0.9263 A 411 ILE 12.9785 6.2633 19.6936 A 412 GLU 16.8133 9.6352 22.5559 A 413 GLY 9.4666 9.4666 0.0000 A 414 GLU 2.5510 2.5156 2.5794 A 415 THR 5.9752 0.0898 13.8224 A 416 TYR 0.5074 0.0226 0.7498 A 417 GLN 7.2197 0.0821 12.9297 A 418 CYS 0.0003 0.0000 0.0009 A 419 ALA 5.4324 0.0002 27.1613 A 420 VAL 0.0672 0.1174 0.0002 A 421 THR 9.2655 0.3477 21.1559 A 422 ALA 3.5044 2.8442 6.1452 A 423 PRO 8.5866 10.2103 6.4216 A 424 ALA 8.3566 3.5672 27.5142 A 425 LEU 11.7212 8.7651 14.6773 A 426 PRO 17.7261 10.5785 27.2562 A 427 ARG 17.5755 2.8707 25.9782 A 428 ALA 9.8149 5.3119 27.8269 A 429 LEU 6.4318 0.7950 12.0687 A 430 MET 15.6753 5.2815 26.0691 A 431 ARG 8.2369 1.4606 12.1090 A 432 SER 12.1223 6.7546 22.8576 A 433 THR 1.7085 1.7868 1.6042 A 434 THR 7.5244 1.8978 15.0265 A 435 ALA 7.7753 3.7138 24.0213 A 436 THR 8.6934 2.5690 16.8594 A 437 SER 15.8041 3.9341 39.5441 A 438 GLY 10.8151 10.8151 0.0000 A 439 PRO 13.4383 3.2705 26.9955 A 440 ARG 8.7641 7.5143 9.4782 A 441 ALA 6.7461 1.8371 26.3821 A 442 ALA 10.4272 3.2972 38.9468 A 443 PRO 1.3762 2.4083 0.0000 A 444 ALA 9.1593 2.0797 37.4777 A 445 VAL 0.9848 1.7231 0.0005 A 446 TYR 3.1461 0.0000 4.7192 A 447 ALA 0.0289 0.0362 0.0000 A 448 PHE 0.6153 0.0000 0.9669 A 449 ALA 3.8692 3.2275 6.4360 A 450 THR 1.9237 0.4303 3.9148 A 451 PRO 12.1453 6.5643 19.5866 A 452 GLU 7.9403 6.9431 8.7381 A 453 ALA 30.2649 20.0784 71.0111 A 459 LYS 14.7292 11.5275 17.2907 A 460 ARG 5.9981 0.0765 9.3819 A 461 THR 0.1536 0.0000 0.3584 A 462 LEU 0.0001 0.0002 0.0000 A 463 ALA 0.0001 0.0001 0.0000 A 464 CYS 0.0087 0.0130 0.0000 A 465 LEU 0.0982 0.1233 0.0732 A 466 ILE 0.0200 0.0000 0.0401 A 467 GLN 0.8305 0.0002 1.4947 A 468 ASN 5.9937 1.5627 10.4246 A 469 PHE 0.0000 0.0000 0.0000 A 470 MET 7.2629 0.0000 14.5258 A 471 PRO 1.8851 1.4594 2.4527 A 472 GLU 7.3364 0.4665 12.8323 A 473 ASP 5.6153 1.4927 9.7380 A 474 ILE 3.5567 6.3075 0.8058 A 475 SER 2.6057 1.5404 4.7363 A 476 VAL 2.4253 3.4886 1.0077 A 477 GLN 1.0498 0.0000 1.8897 A 478 TRP 0.1187 0.2438 0.0687 A 479 LEU 0.6608 0.0000 1.3216 A 480 HIS 5.1342 0.7731 8.0417 A 481 ASN 6.5819 0.8724 12.2914 A 482 GLU 18.7049 10.4001 25.3487 A 483 VAL 12.0619 0.7436 27.1528 A 484 GLN 8.9474 5.5610 11.6565 A 485 LEU 3.1319 1.3283 4.9354 A 486 PRO 12.0736 3.3535 23.7005 A 487 ASP 12.6169 1.7276 23.5062 A 488 ALA 20.4452 11.0832 57.8933 A 489 ARG 7.8562 4.5508 9.7450 A 490 HIS 2.6987 4.4236 1.5488 A 491 SER 4.4347 1.1905 10.9232 A 492 THR 5.2960 2.8369 8.5749 A 493 THR 0.9440 0.7955 1.1420 A 494 GLN 13.6713 0.9109 23.8796 A 495 PRO 6.0581 4.4972 8.1393 A 496 ARG 6.3674 0.9523 9.4618 A 497 LYS 16.8451 3.4562 27.5561 A 498 THR 4.5143 6.9964 1.2047 A 499 ALA 17.0252 11.1864 40.3805 A 500 GLY 18.8178 18.8178 0.0000 A 501 SER 5.4365 3.4214 9.4666 A 502 GLY 2.8894 2.8894 0.0000 A 503 PHE 3.0581 0.0894 4.7545 A 504 PHE 0.0656 0.0228 0.0900 A 505 VAL 0.2424 0.0053 0.5586 A 506 PHE 0.0016 0.0039 0.0003 A 507 SER 0.0350 0.0179 0.0692 A 508 ARG 0.6294 0.6714 0.6054 A 509 LEU 0.0392 0.0185 0.0599 A 510 GLU 1.7287 1.2093 2.1442 A 511 VAL 0.3299 0.5773 0.0000 A 512 THR 10.6447 1.4856 22.8569 A 513 ARG 9.5285 0.8196 14.5051 A 514 ALA 14.8713 4.4288 56.6415 A 515 GLU 3.0827 1.0010 4.7481 A 516 TRP 3.3932 0.5950 4.5125 A 517 GLU 12.8907 5.2405 19.0109 A 518 ALA 5.1774 0.5587 23.6525 A 519 LYS 3.0790 0.0000 5.5422 A 520 ASP 10.4782 3.6427 17.3137 A 521 GLU 7.1047 0.7149 12.2165 A 522 PHE 0.0000 0.0000 0.0001 A 523 ILE 3.5408 0.0000 7.0817 A 524 CYS 0.0000 0.0000 0.0000 A 525 ARG 4.6100 0.0000 7.2442 A 526 ALA 0.0902 0.1128 0.0000 A 527 VAL 0.0669 0.0002 0.1558 A 528 HIS 0.1300 0.0054 0.2131 A 529 GLU 7.9604 2.2867 12.4993 A 530 ALA 4.2802 4.7817 2.2743 A 531 ALA 0.7347 0.7875 0.5235 A 532 SER 15.8770 7.2992 33.0325 A 533 PRO 12.8146 2.0699 27.1409 A 534 SER 13.2955 4.9891 29.9083 A 535 GLN 4.3097 0.0000 7.7574 A 536 THR 5.4579 3.7045 7.7958 A 537 VAL 5.1081 1.4055 10.0450 A 538 GLN 8.2068 4.5359 11.1435 A 539 ARG 10.8337 1.0576 16.4201 A 540 ALA 9.1994 1.8430 38.6251 A 541 VAL 1.0570 1.8498 0.0000 A 542 SER 8.0549 3.4723 17.2202 A 543 VAL 18.5723 20.6424 15.8122 A 2 NAG 16.4353 0.0000 16.4353 B 336 VAL 10.7710 10.1163 11.6438 B 337 SER 6.7303 0.9166 18.3577 B 338 ALA 2.1458 2.6822 0.0000 B 339 TYR 8.0696 1.1676 11.5206 B 340 LEU 3.9394 7.4662 0.4127 B 341 SER 10.1645 1.0695 28.3545 B 342 ARG 6.0757 3.9259 7.3041 B 343 PRO 1.0733 1.5124 0.4878 B 344 SER 7.7643 2.0338 19.2253 B 345 PRO 1.3185 0.0201 3.0497 B 346 PHE 4.8258 0.0000 7.5834 B 347 ASP 3.9197 0.0000 7.8394 B 348 LEU 1.9999 0.7895 3.2104 B 349 PHE 4.1817 4.2283 4.1551 B 350 ILE 7.9930 2.5475 13.4385 B 351 ARG 12.3730 6.6042 15.6695 B 352 LYS 15.0045 3.9474 23.8501 B 353 SER 8.5948 1.6503 22.4838 B 354 PRO 0.2553 0.1754 0.3617 B 355 THR 5.9200 1.2321 12.1705 B 356 ILE 0.1391 0.2781 0.0000 B 357 THR 5.2617 0.3654 11.7900 B 358 CYS 0.0000 0.0000 0.0000 B 359 LEU 3.5340 0.0000 7.0680 B 360 VAL 0.5390 0.0799 1.1511 B 361 VAL 3.7224 0.1093 8.5398 B 362 ASP 1.8094 0.3525 3.2662 B 363 ALA 20.0439 10.4606 58.3772 B 364 ALA 15.3707 4.9576 57.0231 B 365 PRO 9.1152 4.3450 15.4754 B 366 ALA 18.8285 10.0035 54.1287 B 367 LYS 14.1725 9.5150 17.8985 B 368 GLY 19.0630 19.0630 0.0000 B 369 ALA 13.0115 3.7971 49.8693 B 370 VAL 1.7523 0.1998 3.8225 B 371 ASN 10.0509 0.2812 19.8206 B 372 LEU 3.4036 6.2343 0.5729 B 373 THR 11.1077 0.8564 24.7761 B 374 TRP 1.5073 3.6124 0.6652 B 375 SER 8.3615 0.6614 23.7617 B 376 ARG 3.0771 1.9562 3.7176 B 377 ALA 15.1815 11.3744 30.4099 B 378 SER 11.4636 9.9129 14.5651 B 379 GLY 16.5804 16.5804 0.0000 B 380 LYS 13.2366 1.9343 22.2785 B 381 PRO 15.6715 3.5998 31.7671 B 382 VAL 7.5283 6.2163 9.2776 B 383 ASN 11.4020 3.4390 19.3649 B 384 HIS 17.6888 3.0947 27.4182 B 385 SER 9.0145 7.7907 11.4622 B 386 THR 10.6406 1.1756 23.2606 B 387 ARG 8.8774 6.6756 10.1356 B 388 LYS 12.6102 1.7918 21.2649 B 389 GLU 12.4839 8.7255 15.4906 B 390 ALA 12.8869 2.5604 54.1927 B 391 ALA 27.0786 21.9964 47.4075 B 397 LEU 7.6502 6.6415 8.6588 B 398 THR 5.7838 0.0392 13.4434 B 399 VAL 0.3391 0.0000 0.7912 B 400 THR 3.3805 0.0000 7.8879 B 401 SER 0.7193 0.0000 2.1579 B 402 THR 3.7007 0.2432 8.3106 B 403 LEU 0.1106 0.0003 0.2208 B 404 PRO 8.1540 0.8611 17.8779 B 405 VAL 1.5566 2.7241 0.0000 B 406 GLY 7.1791 7.1791 0.0000 B 407 THR 7.0853 0.8445 15.4063 B 408 ALA 12.2481 1.5500 55.0403 B 409 ASP 7.3052 0.7230 13.8873 B 410 TRP 0.6460 0.0006 0.9042 B 411 ILE 12.7563 5.8221 19.6905 B 412 GLU 16.8891 9.7584 22.5936 B 413 GLY 9.7410 9.7410 0.0000 B 414 GLU 2.5752 2.6119 2.5458 B 415 THR 5.4692 0.0703 12.6676 B 416 TYR 0.4512 0.0209 0.6663 B 417 GLN 7.0959 0.0872 12.7029 B 418 CYS 0.0000 0.0000 0.0000 B 419 ALA 5.4563 0.0000 27.2815 B 420 VAL 0.0843 0.1418 0.0075 B 421 THR 9.3197 0.3238 21.3142 B 422 ALA 3.6164 3.0205 6.0000 B 423 PRO 8.4785 10.2004 6.1826 B 424 ALA 8.6226 3.5932 28.7401 B 425 LEU 11.9869 8.8343 15.1395 B 426 PRO 17.5822 10.4491 27.0930 B 427 ARG 17.4020 2.6803 25.8144 B 428 ALA 9.7570 5.0751 28.4846 B 429 LEU 6.0642 0.7211 11.4073 B 430 MET 16.0818 5.9456 26.2180 B 431 ARG 8.0744 1.6123 11.7671 B 432 SER 12.2372 6.6046 23.5024 B 433 THR 1.4684 1.6247 1.2601 B 434 THR 7.3739 1.2286 15.5676 B 435 ALA 7.8667 3.8619 23.8858 B 436 THR 8.4287 2.5153 16.3133 B 437 SER 15.9443 4.0579 39.7171 B 438 GLY 10.6293 10.6293 0.0000 B 439 PRO 13.9484 3.3166 28.1241 B 440 ARG 8.8462 7.2368 9.7658 B 441 ALA 6.9507 1.8590 27.3179 B 442 ALA 10.4125 3.4391 38.3062 B 443 PRO 1.4008 2.4371 0.0192 B 444 ALA 9.0537 2.0618 37.0209 B 445 VAL 1.0436 1.8263 0.0000 B 446 TYR 3.2280 0.0004 4.8418 B 447 ALA 0.0363 0.0454 0.0000 B 448 PHE 0.6260 0.0000 0.9837 B 449 ALA 3.9414 3.2169 6.8396 B 450 THR 2.0045 0.4174 4.1205 B 451 PRO 12.0887 6.8483 19.0759 B 452 GLU 8.1587 7.1306 8.9811 B 453 ALA 30.2751 20.7889 68.2199 B 459 LYS 14.9002 12.1326 17.1143 B 460 ARG 6.1453 0.0029 9.6552 B 461 THR 0.1144 0.0006 0.2661 B 462 LEU 0.0002 0.0003 0.0000 B 463 ALA 0.0000 0.0000 0.0000 B 464 CYS 0.0113 0.0170 0.0000 B 465 LEU 0.0910 0.0946 0.0874 B 466 ILE 0.0219 0.0000 0.0437 B 467 GLN 0.8389 0.0000 1.5100 B 468 ASN 5.9301 1.4721 10.3881 B 469 PHE 0.0000 0.0000 0.0000 B 470 MET 7.0813 0.0000 14.1626 B 471 PRO 1.8331 1.3727 2.4469 B 472 GLU 7.3943 0.5175 12.8958 B 473 ASP 5.5075 1.5025 9.5124 B 474 ILE 3.5810 6.3586 0.8033 B 475 SER 2.6182 1.5408 4.7731 B 476 VAL 2.3682 3.3339 1.0806 B 477 GLN 1.0871 0.0000 1.9567 B 478 TRP 0.1016 0.2324 0.0492 B 479 LEU 0.5440 0.0000 1.0880 B 480 HIS 5.2031 0.7382 8.1798 B 481 ASN 6.8401 0.8806 12.7996 B 482 GLU 19.0404 11.1613 25.3436 B 483 VAL 11.8885 0.8953 26.5460 B 484 GLN 8.9330 5.5624 11.6295 B 485 LEU 2.9872 1.1924 4.7819 B 486 PRO 12.4420 3.2393 24.7123 B 487 ASP 12.6235 1.8226 23.4245 B 488 ALA 20.9557 11.2245 59.8807 B 489 ARG 7.5032 4.6052 9.1591 B 490 HIS 2.6761 4.4041 1.5240 B 491 SER 4.3984 1.1740 10.8470 B 492 THR 5.2933 2.7736 8.6528 B 493 THR 0.8019 0.6773 0.9680 B 494 GLN 13.6817 0.8084 23.9803 B 495 PRO 5.9741 4.5062 7.9314 B 496 ARG 6.4874 0.9751 9.6372 B 497 LYS 16.4562 3.2776 26.9991 B 498 THR 4.6427 7.1707 1.2720 B 499 ALA 17.5008 11.3708 42.0207 B 500 GLY 18.7401 18.7401 0.0000 B 501 SER 5.4215 3.4199 9.4248 B 502 GLY 2.8691 2.8691 0.0000 B 503 PHE 2.9965 0.0437 4.6838 B 504 PHE 0.0651 0.0203 0.0907 B 505 VAL 0.2042 0.0000 0.4765 B 506 PHE 0.0052 0.0143 0.0000 B 507 SER 0.0331 0.0000 0.0993 B 508 ARG 0.5554 0.6385 0.5080 B 509 LEU 0.0476 0.0286 0.0666 B 510 GLU 1.7117 1.1583 2.1544 B 511 VAL 0.3510 0.6142 0.0000 B 512 THR 10.6600 1.5410 22.8185 B 513 ARG 9.4359 0.8028 14.3691 B 514 ALA 15.2935 4.4804 58.5460 B 515 GLU 2.9658 1.4237 4.1995 B 516 TRP 3.3612 0.5404 4.4896 B 517 GLU 12.5876 4.9796 18.6740 B 518 ALA 4.6347 0.6025 20.7633 B 519 LYS 2.7664 0.0000 4.9795 B 520 ASP 10.6223 3.6037 17.6410 B 521 GLU 7.3610 0.6603 12.7216 B 522 PHE 0.0081 0.0000 0.0128 B 523 ILE 3.5242 0.0007 7.0477 B 524 CYS 0.0000 0.0000 0.0000 B 525 ARG 4.7547 0.0000 7.4716 B 526 ALA 0.0709 0.0887 0.0000 B 527 VAL 0.0762 0.0000 0.1777 B 528 HIS 0.1255 0.0005 0.2088 B 529 GLU 7.9368 2.2949 12.4503 B 530 ALA 4.2207 4.6880 2.3517 B 531 ALA 0.7409 0.8075 0.4746 B 532 SER 16.1085 7.5394 33.2468 B 533 PRO 13.1853 2.0824 27.9892 B 534 SER 13.2835 4.9738 29.9029 B 535 GLN 4.1001 0.0000 7.3802 B 536 THR 5.5193 3.5752 8.1115 B 537 VAL 5.1049 1.4593 9.9656 B 538 GLN 8.2211 4.4767 11.2166 B 539 ARG 10.8149 1.1022 16.3650 B 540 ALA 8.9590 1.8529 37.3835 B 541 VAL 1.0803 1.8905 0.0000 B 542 SER 8.4553 4.0882 17.1897 B 543 VAL 18.5355 20.8533 15.4451 B 2 NAG 16.5934 0.0000 16.5934

[0048] In another embodiment, the solvent accessibilities of the amino acids in PhFc-Cε3/Cε4₁₋₂₂₂ are indicated in Table 5. TABLE 5 IgE-Fc Residue Exposure >>>> Surface plot for: >>>> structure file = 1FP5_easy.mtf >>>> coordinate set = 1FP5_easy.pdb total accessible area segid resid resname residue mainchain sidechain A 336 VAL 64.9492 37.4745 27.4746 A 337 SER 39.1673 3.9332 35.2340 A 338 ALA 8.7894 8.7894 0.0000 A 339 TYR 125.2426 4.9472 120.2955 A 340 LEU 29.8639 28.5555 1.3085 A 341 SER 61.1170 4.9569 56.1601 A 342 ARG 65.4430 15.2049 50.2381 A 343 PRO 7.4718 5.8928 1.5790 A 344 SER 46.7157 8.2264 38.4893 A 345 PRO 8.9624 0.1428 8.8196 A 346 PHE 54.3420 0.0000 54.3420 A 347 ASP 31.5363 0.0000 31.5363 A 348 LEU 7.5406 3.0628 4.4778 A 349 PHE 47.0594 17.8090 29.2504 A 350 ILE 65.6199 9.9606 55.6593 A 351 ARG 137.9028 24.7368 113.1660 A 352 LYS 142.0125 20.1726 121.8399 A 353 SER 48.9241 7.6848 41.2393 A 354 PRO 2.7838 1.3055 1.4783 A 355 THR 40.4021 4.8060 35.5961 A 356 ILE 0.7303 0.7288 0.0015 A 357 THR 38.1965 1.6685 36.5281 A 358 CYS 0.0000 0.0000 0.0000 A 359 LEU 57.2918 0.0000 57.2918 A 360 VAL 1.4811 0.0000 1.4811 A 361 VAL 26.4275 0.0000 26.4275 A 362 ASP 1.6559 0.0000 1.6559 A 363 LEU 119.6712 9.2033 110.4678 A 364 ALA 78.7333 14.3696 64.3637 A 365 PRO 79.3853 32.3651 47.0202 A 366 SER 40.2168 14.0242 26.1926 A 367 LYS 212.4325 43.2686 169.1639 A 368 GLY 39.8856 39.8856 0.0000 A 369 THR 102.7635 12.0075 90.7560 A 370 VAL 5.8020 1.2971 4.5049 A 371 ASN 70.8195 0.5930 70.2265 A 372 LEU 26.6375 25.3607 1.2768 A 373 THR 63.8640 3.8953 59.9687 A 374 TRP 19.5203 12.4611 7.0592 A 375 SER 49.4189 2.7649 46.6540 A 376 ARG 31.0928 7.7441 23.3486 A 377 ALA 77.5219 45.8060 31.7159 A 378 SER 66.6797 40.4771 26.2025 A 379 GLY 65.8988 65.8988 0.0000 A 380 LYS 116.4270 8.7936 107.6334 A 381 PRO 108.8295 14.6070 94.2226 A 382 VAL 54.2349 26.8569 27.3780 A 383 ASN 86.4753 13.4514 73.0239 A 384 HIS 173.6417 12.7135 160.9282 A 385 SER 51.7955 28.3694 23.4261 A 386 THR 72.2038 3.6585 68.5453 A 387 ARG 97.7388 26.1865 71.5523 A 388 LYS 115.4839 6.8986 108.5853 A 389 GLU 113.2234 35.2996 77.9238 A 390 GLU 116.4752 6.3676 110.1076 A 391 LYS 144.4826 24.7116 119.7710 A 392 GLN 113.9451 7.7214 106.2237 A 393 ARG 217.0740 36.0558 181.0182 A 394 ASN 127.4447 33.3744 94.0703 A 395 GLY 23.5351 23.5351 0.0000 A 396 THR 35.9405 2.2916 33.6489 A 397 LEU 37.3071 0.3897 36.9174 A 398 THR 36.6338 0.1084 36.5254 A 399 VAL 1.0056 0.0005 1.0051 A 400 THR 22.9397 0.0005 22.9392 A 401 SER 4.2325 0.0010 4.2315 A 402 THR 25.0142 0.7905 24.2237 A 403 LEU 1.2610 0.0000 1.2610 A 404 PRO 55.8249 3.3119 52.5130 A 405 VAL 10.7120 10.7120 0.0000 A 406 GLY 30.1703 30.1703 0.0000 A 407 THR 48.6461 5.0988 43.5474 A 408 ARG 142.5092 1.0113 141.4979 A 409 ASP 56.6478 3.0794 53.5684 A 410 TRP 1.0792 0.0006 1.0786 A 411 ILE 66.2093 21.0455 45.1638 A 412 GLU 145.4881 39.5895 105.8986 A 413 GLY 38.6895 38.6895 0.0000 A 414 GLU 22.1923 9.2475 12.9448 A 415 THR 40.6026 0.2438 40.3588 A 416 TYR 5.1230 0.0308 5.0922 A 417 GLN 62.3280 0.4057 61.9222 A 418 CYS 0.0000 0.0000 0.0000 A 419 ARG 103.9206 0.0000 103.9206 A 420 VAL 2.3852 1.4107 0.9744 A 421 THR 46.0180 1.1126 44.9053 A 422 HIS 16.6307 8.9744 7.6562 A 423 PRO 63.0244 42.0681 20.9562 A 424 HIS 126.3997 30.4096 95.9901 A 425 LEU 73.4692 13.0120 60.4572 A 426 PRO 136.4835 43.7065 92.7770 A 427 ARG 174.1798 16.4322 157.7477 A 428 ALA 31.7676 12.1334 19.6342 A 429 LEU 47.6693 3.3487 44.3206 A 430 MET 81.9649 21.6349 60.3301 A 431 ARG 102.1664 3.7496 98.4168 A 432 SER 74.7559 27.6174 47.1385 A 433 THR 12.0200 7.4697 4.5502 A 434 THR 54.0747 7.5188 46.5559 A 435 LYS 39.4746 13.2184 26.2562 A 436 THR 54.0546 6.8840 47.1706 A 437 SER 92.5356 13.8146 78.7209 A 438 GLY 44.5439 44.5439 0.0000 A 439 PRO 95.9599 12.1244 83.8355 A 440 ARG 85.9106 27.8327 58.0779 A 441 ALA 31.0495 7.8868 23.1627 A 442 ALA 52.0384 13.4854 38.5529 A 443 PRO 9.0934 9.0918 0.0015 A 444 GLU 50.5501 4.8813 45.6687 A 445 VAL 1.1996 1.1993 0.0004 A 446 TYR 33.1189 0.0000 33.1189 A 447 ALA 0.2103 0.2103 0.0000 A 448 PHE 6.4091 0.0021 6.4070 A 449 ALA 18.5169 13.0271 5.4898 A 450 THR 6.8652 1.0920 5.7732 A 451 PRO 85.0090 26.0777 58.9313 A 452 GLU 53.5564 21.4659 32.0906 A 453 TRP 233.7213 21.0784 212.6428 A 454 PRO 110.0223 22.9884 87.0339 A 455 GLY 58.2985 58.2985 0.0000 A 456 SER 83.8465 35.4457 48.4007 A 457 ARG 204.5646 33.7345 170.8301 A 458 ASP 74.3533 35.5320 38.8213 A 459 LYS 90.8795 5.6494 85.2301 A 460 ARG 39.6337 0.3815 39.2522 A 461 THR 0.9440 0.0000 0.9440 A 462 LEU 0.0000 0.0000 0.0000 A 463 ALA 0.0022 0.0022 0.0000 A 464 CYS 0.0189 0.0189 0.0000 A 465 LEU 0.0024 0.0000 0.0024 A 466 ILE 0.0969 0.0000 0.0969 A 467 GLN 4.2986 0.0000 4.2986 A 468 ASN 45.2933 4.2260 41.0673 A 469 PHE 0.0016 0.0000 0.0016 A 470 MET 45.6193 0.0006 45.6187 A 471 PRO 10.5390 4.5735 5.9655 A 472 GLU 66.1010 1.3044 64.7966 A 473 ASP 34.3329 6.6650 27.6679 A 474 ILE 28.1949 24.7847 3.4102 A 475 SER 15.8011 5.8009 10.0002 A 476 VAL 17.7598 14.8483 2.9115 A 477 GLN 8.8153 0.0008 8.8145 A 478 TRP 1.6124 0.9129 0.6996 A 479 LEU 3.6886 0.0000 3.6886 A 480 HIS 49.2343 0.4256 48.8086 A 481 ASN 60.9710 12.4862 48.4849 A 482 GLU 173.7820 37.6217 136.1603 A 483 VAL 89.3318 4.1549 85.1769 A 484 GLN 79.3073 21.3545 57.9528 A 485 LEU 27.3587 5.2803 22.0784 A 486 PRO 88.6492 13.2533 75.3958 A 487 ASP 99.0020 6.5842 92.4178 A 488 ALA 91.2923 30.7006 60.5917 A 489 ARG 85.3735 17.3474 68.0262 A 490 HIS 27.1818 17.0174 10.1644 A 491 SER 25.4648 5.3465 20.1183 A 492 THR 37.6322 11.4738 26.1583 A 493 THR 6.2876 3.0406 3.2469 A 494 GLN 120.0995 2.7999 117.2995 A 495 PRO 41.3128 17.2964 24.0164 A 496 ARG 67.3088 3.7186 63.5902 A 497 LYS 150.2799 14.2135 136.0663 A 498 THR 38.1648 34.4749 3.6899 A 499 LYS 148.5493 8.5618 139.9875 A 500 GLY 76.9764 76.9764 0.0000 A 501 SER 35.3537 27.8013 7.5524 A 502 GLY 8.6018 8.6018 0.0000 A 503 PHE 31.7527 1.3561 30.3966 A 504 PHE 0.8997 0.1297 0.7700 A 505 VAL 1.3819 0.0043 1.3776 A 506 PHE 0.0393 0.0393 0.0000 A 507 SER 0.0697 0.0697 0.0000 A 508 ARG 7.6439 2.8043 4.8396 A 509 LEU 0.3316 0.0344 0.2972 A 510 GLU 22.5879 7.4305 15.1574 A 511 VAL 7.0471 7.0471 0.0000 A 512 THR 80.5746 7.4380 73.1367 A 513 ARG 111.1689 3.1148 108.0541 A 514 ALA 58.1366 5.4416 52.6950 A 515 GLU 27.2188 0.1935 27.0253 A 516 TRP 44.3047 2.1698 42.1350 A 517 GLU 113.2078 31.9303 81.2775 A 518 GLN 44.8077 1.3672 43.4405 A 519 LYS 31.0147 0.0000 31.0147 A 520 ASP 84.0782 14.7455 69.3327 A 521 GLU 67.8496 3.1378 64.7117 A 522 PHE 2.3708 0.0000 2.3708 A 523 ILE 19.4152 0.0000 19.4152 A 524 CYS 0.0000 0.0000 0.0000 A 525 ARG 53.8480 0.0000 53.8480 A 526 ALA 0.1543 0.1521 0.0022 A 527 VAL 0.4091 0.0000 0.4091 A 528 HIS 0.9368 0.0000 0.9368 A 529 GLU 49.8255 6.7170 43.1084 A 530 ALA 25.3085 22.0423 3.2662 A 531 ALA 3.8937 3.7960 0.0977 A 532 SER 93.9367 25.5989 68.3378 A 533 PRO 113.4963 7.9201 105.5762 A 534 SER 69.1432 17.4384 51.7047 A 535 GLN 39.0154 0.0000 39.0154 A 536 THR 47.4246 15.9885 31.4361 A 537 VAL 37.3796 5.2662 32.1134 A 538 GLN 80.4137 17.3329 63.0807 A 539 ARG 114.1401 5.3396 108.8005 A 540 ALA 46.1789 7.2011 38.9778 A 541 VAL 7.4375 7.4375 0.0000 A 542 SER 53.4887 16.3308 37.1580 A 543 VAL 143.3700 54.8988 88.4713 B 336 VAL 63.0733 35.0684 28.0049 B 337 SER 40.7513 3.7350 37.0163 B 338 ALA 8.2164 8.2164 0.0000 B 339 TYR 124.9616 4.9609 120.0006 B 340 LEU 32.2736 30.2378 2.0358 B 341 SER 59.0456 4.4001 54.6455 B 342 ARG 68.6573 15.2123 53.4449 B 343 PRO 7.5644 6.0344 1.5300 B 344 SER 46.7394 8.2658 38.4735 B 345 PRO 8.8647 0.0661 8.7987 B 346 PHE 52.7081 0.0001 52.7079 B 347 ASP 32.0935 0.0000 32.0935 B 348 LEU 14.8371 3.0411 11.7960 B 349 PHE 49.2963 17.4349 31.8613 B 350 ILE 66.6755 11.3996 55.2758 B 351 ARG 138.6156 27.1648 111.4508 B 352 LYS 141.4297 19.8862 121.5435 B 353 SER 50.0186 7.0285 42.9901 B 354 PRO 2.2374 0.7342 1.5032 B 355 THR 41.7632 5.0415 36.7217 B 356 ILE 0.7365 0.7350 0.0014 B 357 THR 38.2632 1.6972 36.5659 B 358 CYS 0.0000 0.0000 0.0000 B 359 LEU 56.1126 0.0000 56.1126 B 360 VAL 1.5816 0.0000 1.5816 B 361 VAL 25.9197 0.0054 25.9143 B 362 ASP 1.8960 0.0000 1.8960 B 363 LEU 118.5662 9.4704 109.0958 B 364 ALA 77.0955 14.3989 62.6966 B 365 PRO 85.8755 32.6618 53.2137 B 366 SER 43.4697 13.7975 29.6721 B 367 LYS 206.9839 38.4032 168.5807 B 368 GLY 38.3029 38.3029 0.0000 B 369 THR 104.4643 11.7881 92.6762 B 370 VAL 5.3648 1.3354 4.0294 B 371 ASN 71.8454 0.6766 71.1688 B 372 LEU 27.2777 25.4561 1.8216 B 373 THR 63.4130 3.0688 60.3442 B 374 TRP 21.1747 14.5837 6.5910 B 375 SER 49.3968 2.8090 46.5877 B 376 ARG 33.5679 7.8441 25.7238 B 377 ALA 75.8852 45.5987 30.2865 B 378 SER 67.8229 40.7526 27.0703 B 379 GLY 66.3404 66.3404 0.0000 B 380 LYS 120.5164 9.2949 111.2215 B 381 PRO 109.6176 14.2385 95.3791 B 382 VAL 53.1169 25.2918 27.8251 B 383 ASN 91.8842 12.6656 79.2186 B 384 HIS 177.7631 13.1140 164.6491 B 385 SER 54.1445 30.9373 23.2073 B 386 THR 75.0451 3.9383 71.1068 B 387 ARG 103.3354 27.2889 76.0466 B 388 LYS 118.3613 6.6694 111.6919 B 389 GLU 102.2353 27.4529 74.7824 B 390 GLU 111.8330 2.2529 109.5801 B 391 LYS 164.3363 16.4358 147.9005 B 392 GLN 115.7355 9.9426 105.7929 B 393 ARG 243.1959 43.7367 199.4592 B 394 ASN 128.7879 34.6864 94.1016 B 395 GLY 24.2780 24.2780 0.0000 B 396 THR 36.3774 3.2281 33.1493 B 397 LEU 41.3144 1.2301 40.0844 B 398 THR 36.2084 0.1877 36.0207 B 399 VAL 0.9349 0.0000 0.9349 B 400 THR 22.7308 0.0000 22.7308 B 401 SER 4.4619 0.0000 4.4619 B 402 THR 26.2017 0.7838 25.4179 B 403 LEU 1.0199 0.0000 1.0199 B 404 PRO 56.9154 3.8109 53.1046 B 405 VAL 12.3109 12.3109 0.0000 B 406 GLY 29.3614 29.3614 0.0000 B 407 THR 42.7403 3.8469 38.8934 B 408 ARG 157.6823 3.1126 154.5697 B 409 ASP 51.4385 3.0432 48.3953 B 410 TRP 9.3345 0.0000 9.3345 B 411 ILE 95.1467 19.7743 75.3724 B 412 GLU 125.4698 37.7238 87.7460 B 413 GLY 18.7812 18.7812 0.0000 B 414 GLU 22.6140 9.6511 12.9629 B 415 THR 39.5185 0.3206 39.1980 B 416 TYR 5.9881 0.0409 5.9472 B 417 GLN 62.6966 0.3477 62.3489 B 418 CYS 0.0000 0.0000 0.0000 B 419 ARG 102.6084 0.0000 102.6084 B 420 VAL 2.7707 1.6846 1.0861 B 421 THR 46.0095 0.8195 45.1900 B 422 HIS 16.7868 8.9411 7.8457 B 423 PRO 62.8378 41.9162 20.9217 B 424 HIS 125.3588 30.3775 94.9814 B 425 LEU 71.5870 12.6261 58.9609 B 426 PRO 136.6526 45.8124 90.8402 B 427 ARG 170.2552 16.6453 153.6099 B 428 ALA 32.0708 12.4769 19.5939 B 429 LEU 48.8898 2.1566 46.7332 B 430 MET 84.2805 22.5773 61.7032 B 431 ARG 100.5128 3.0888 97.4240 B 432 SER 75.1133 26.0086 49.1047 B 433 THR 10.4817 6.7238 3.7580 B 434 THR 48.7159 5.3780 43.3380 B 435 LYS 72.0172 7.7237 64.2934 B 436 THR 58.8140 9.6274 49.1866 B 437 SER 83.7729 12.9694 70.8035 B 438 GLY 44.1275 44.1275 0.0000 B 439 PRO 98.8394 12.2219 86.6175 B 440 ARG 88.9167 29.3709 59.5458 B 441 ALA 32.3694 7.8101 24.5593 B 442 ALA 52.2561 13.8471 38.4090 B 443 PRO 9.1527 9.0687 0.0839 B 444 GLU 77.6629 1.5591 76.1038 B 445 VAL 2.0960 2.0960 0.0000 B 446 TYR 36.2935 0.0000 36.2935 B 447 ALA 0.1863 0.1863 0.0000 B 448 PHE 6.5491 0.0000 6.5491 B 449 ALA 18.6090 12.5251 6.0838 B 450 THR 4.4299 1.1588 3.2711 B 451 PRO 76.6290 22.7457 53.8833 B 452 GLU 55.5072 22.2581 33.2491 B 453 TRP 235.9264 21.1124 214.8139 B 454 PRO 111.4380 22.8008 88.6373 B 455 GLY 74.9059 74.9059 0.0000 B 456 SER 92.2118 45.4910 46.7208 B 457 ARG 219.5241 23.6314 195.8927 B 458 ASP 71.4157 34.5621 36.8536 B 459 LYS 95.3227 8.3619 86.9608 B 460 ARG 40.1231 0.1393 39.9838 B 461 THR 1.4382 0.0000 1.4382 B 462 LEU 0.0000 0.0000 0.0000 B 463 ALA 0.0000 0.0000 0.0000 B 464 CYS 0.0199 0.0199 0.0000 B 465 LEU 0.7613 0.4703 0.2910 B 466 ILE 0.1384 0.0000 0.1384 B 467 GLN 6.3987 0.0000 6.3987 B 468 ASN 44.9702 3.7128 41.2575 B 469 PHE 0.0026 0.0000 0.0026 B 470 MET 46.3764 0.0005 46.3759 B 471 PRO 15.0525 5.0794 9.9731 B 472 GLU 65.5924 1.4428 64.1496 B 473 ASP 46.5992 6.7495 39.8497 B 474 ILE 28.5269 25.0290 3.4979 B 475 SER 15.9668 5.7847 10.1821 B 476 VAL 17.4473 14.3713 3.0760 B 477 GLN 9.3877 0.0000 9.3877 B 478 TRP 1.3921 0.8722 0.5198 B 479 LEU 4.3690 0.0000 4.3690 B 480 HIS 54.2843 0.6477 53.6366 B 481 ASN 58.4959 9.8012 48.6946 B 482 GLU 167.3206 33.4531 133.8675 B 483 VAL 89.2539 4.2127 85.0413 B 484 GLN 76.3506 21.2575 55.0931 B 485 LEU 25.8432 4.5546 21.2886 B 486 PRO 85.9602 12.9613 72.9989 B 487 ASP 101.5779 6.8540 94.7239 B 488 ALA 89.7437 31.7759 57.9678 B 489 ARG 83.4391 17.2390 66.2001 B 490 HIS 27.4157 17.3316 10.0841 B 491 SER 24.9127 5.0237 19.8890 B 492 THR 37.6675 11.4176 26.2499 B 493 THR 5.6950 2.6368 3.0582 B 494 GLN 117.7065 3.0565 114.6500 B 495 PRO 40.3432 17.1857 23.1575 B 496 ARG 70.2823 3.8397 66.4426 B 497 LYS 150.2087 14.1413 136.0674 B 498 THR 37.9054 34.1687 3.7367 B 499 LYS 148.9955 8.7157 140.2798 B 500 GLY 79.0145 79.0145 0.0000 B 501 SER 35.5772 28.0187 7.5585 B 502 GLY 8.7428 8.7428 0.0000 B 503 PHE 31.0098 0.6811 30.3286 B 504 PHE 0.8456 0.1156 0.7300 B 505 VAL 1.3055 0.0259 1.2796 B 506 PHE 0.0679 0.0679 0.0000 B 507 SER 0.1087 0.0000 0.1087 B 508 ARG 7.6625 2.7772 4.8853 B 509 LEU 0.2769 0.0638 0.2131 B 510 GLU 23.9603 7.2457 16.7146 B 511 VAL 7.2569 7.2569 0.0000 B 512 THR 80.3374 7.5753 72.7621 B 513 ARG 111.7661 3.0775 108.6887 B 514 ALA 68.3844 10.3023 58.0821 B 515 GLU 28.0062 5.9456 22.0606 B 516 TRP 44.6731 2.2532 42.4200 B 517 GLU 101.0924 22.5848 78.5077 B 518 GLN 79.1739 0.0000 79.1739 B 519 LYS 30.5550 0.0000 30.5550 B 520 ASP 81.7324 14.5855 67.1468 B 521 GLU 51.8306 4.1150 47.7156 B 522 PHE 1.2433 0.0000 1.2433 B 523 ILE 27.5515 0.0013 27.5502 B 524 CYS 0.0000 0.0000 0.0000 B 525 ARG 53.0495 0.0000 53.0495 B 526 ALA 0.0470 0.0470 0.0000 B 527 VAL 0.5077 0.0000 0.5077 B 528 HIS 0.8503 0.0026 0.8477 B 529 GLU 70.9722 6.7364 64.2357 B 530 ALA 24.8160 21.6506 3.1654 B 531 ALA 3.8910 3.8714 0.0196 B 532 SER 93.3813 26.2679 67.1135 B 533 PRO 112.7473 7.5061 105.2412 B 534 SER 69.2111 17.8241 51.3871 B 535 GLN 38.1066 0.0000 38.1066 B 536 THR 43.5047 15.6901 27.8146 B 537 VAL 37.1147 5.1494 31.9653 B 538 GLN 75.6644 17.3404 58.3241 B 539 ARG 106.7137 5.0454 101.6683 B 540 ALA 44.2412 8.0048 36.2363 B 541 VAL 7.5264 7.5264 0.0000 B 542 SER 52.7855 16.1622 36.6233 B 543 VAL 145.3042 56.7124 88.5918

[0049] Residues that are solvent accessible are important as they represent amino acids that are on the external surface of the protein and, as such, may be involved in binding of a FcR to an antibody and be useful in designing proteins with an enhanced binding activity or in identifying compounds that inhibit such binding. In addition, solvent accessible residues can represent targets for modification to produce a Fc region of an antibody with improved function. Such analysis also identifies residues in the interior, or core, of the proteins in the complex. Such residues can also be targeted to produce proteins with improved functions, such as enhanced stability.

[0050] A model of the present invention also provides additional information that is not available from other sources. For example, a model can identify the crystal contacts between crystals and predict the location of the FcR binding domain, including those amino acids that actually form contacts with a FcR. Particularly important regions of the model representing the coordinates of Table 1, Table 2 or Table 3 include, but are not limited to the interdomain groove (i.e., space, gap) between the two Cε3/Cε4-containing chains of the IgE antibody Fc region, the hinge between the Cε3 and Cε4 domains of the Fc region, and a loop involved in FcεRIα protein binding, such as the linker between Cε2 and Cε3, the BC loop of Cε3, the DE loop of Cε3, and the FG loop of Cε3. These sites are described in more detail in the Examples and represent sites to target for drug design and mutein production.

[0051] A model of the present invention can also represent a complex that includes a Fc domain of an antibody that binds to a FcεRIα protein with an affinity that is at least equivalent to the affinity of a human IgE antibody Fc-Cε3/Cε4 region for the extracellular domain of any of the following FcεRIα proteins: a human FcεRIα protein, a canine FcεRIα protein, a feline FcεRIα protein, an equine FcεRIα protein, a murine FcεRIα protein and a rat FcεRIα protein. Such a model can represent a FceRI-binding domain of a human, canine, feline, equine, murine or rat Fc region. Such a model can also represent a Fc region with altered substrate specificity, preferably designed based on a model of the present invention.

[0052] The present invention includes a model that represents a Fc domain that binds to a Fc receptor of its respective class. Also included is a model that represents a Fc region of an antibody designed to bind to a Fc receptor of a class other than the class to which the protein naturally binds. Such classes include IgA, IgD, IgE, IgG, and IgM. Such a model of the present invention can be produced, for example, by incorporating all or any part of the amino acid sequence of the other antibody into a 3-D model substantially representing the coordinates in Table 1, Table 2 or Table 3. Such an embodiment includes any model that specifically incorporates any Ig domains that are placed in an orientation (packing interfaces and bend angles) that is based on the structure predicted by the coordinates in Table 1, Table 2 or Table 3 or a similar structure such that the distance between the two antibody-binding domains (i.e., Cε3 for IgE) ranges from about 10 angstroms to about 25 angstroms or from about 20 angstroms to about 40 angstroms. As such, both open and closed conformations of Fc regions are included in the present invention. In one embodiment, a model of the present invention is a 3-D model of a FcεRIα binding domain other than a human FcεRIα binding domain. Such proteins and models thereof can be designed by homology modeling.

[0053] A preferred modified model of the present invention is a model that has a 3-D structure comprising atomic coordinates that have a root mean square deviation of protein backbone atoms of less than 10 angstrom when superimposed, using backbone atoms, on the 3-D model substantially represented by the atomic coordinates specified in Table 1, Table 2 or Table 3. Preferably such a model has a 3-D structure comprising atomic coordinates that have a root mean square deviation of protein backbone atoms of less than 8 angstroms, preferably less than 7 angstroms, preferably less than 6 angstroms, preferably less than 5 angstroms, preferably less than 4 angstroms, preferably less than 3 angstroms, preferably less than 2 angstroms, and preferably less than I angstroms, when superimposed, using backbone atoms, on the 3-D model substantially represented by the atomic coordinates specified in Table 1, Table 2 or Table 3. In this embodiment, such a model represents a Fc region binding to a FcR. The backbone atoms are those atoms that form the backbone, or 3-D folding pattern, of the model. As such, backbone atoms are the base residues of amino acids, i.e., nitrogen, carbon, the alpha carbon and oxygen. Also preferred is a model modification that includes a Fc region having an amino acid sequence that shares at least about 30%, preferably at least about 40%, more preferably at least about 45%, more preferably at least about 50%, more preferably at least about 60% and even more preferably at least about 80% amino acid sequence homology, with a Fc-Cε3/Cε4 region of a human IgE antibody, as determined using the program ALIGN with default parameters, optimal global alignment of two sequences with no short-cuts. A preferred model of the present invention represents a FcεRIα-binding domain, i.e., a region that binds to a FcεRIα protein.

[0054] One embodiment of the present invention is a 3-D model of a human Fc-Cε3/Cε4 region produced by a method that includes the steps of: (a) crystallizing a human Fc-Cε3/Cε4 region, such as, but not limited to a protein having amino acid sequence SEQ ID NO:2; (b) collecting X-ray diffraction data from the crystallized protein; and (c) determining the model from the X-ray diffraction data, preferably in combination with an amino acid sequence of the protein. A complex for crystal formation can be produced using a variety of techniques well known to those skilled in the art. As disclosed herein, a human Fc-Cε3/Cε4 region to be crystallized is preferably produced in recombinant insect cells transformed with a gene encoding such a region, such as a baculovirus genetically engineered to produce the respective protein. The purity of the Fc-Cε3/Cε4 region must be sufficient to permit the production of crystals that can be analyzed by X-ray crystallography to a resolution that permits determination of a 3-D model of the protein. Preferably the resolution is at least about 4.5 angstroms (i.e., 4.4 angstroms or better), more preferably at least about 4 angstroms, more preferably at least about 3.5 angstroms, more preferably at least about 3.25 angstroms, more preferably at least about 3 angstroms, more preferably at least about 2.5 angstroms, more preferably at least about 2.3 angstroms, more preferably at least about 2 angstroms and even more preferably at least about 1.5 angstroms. Methods to obtain such purity levels are well known to those skilled in the art.

[0055] As disclosed herein, a preferred method to crystallize a Fc-Cε3/Cε4 region is by vapor distillation. Particularly preferred methods are disclosed in the Examples. It should be appreciated that the present invention also includes other methods known to those skilled in the art by which such a complex can be crystallized.

[0056] 3-D models of some proteins have been determined; see, for example, Blundell et al., Protein Crystallography, Academic Press, London, 1976. However, as discussed herein, elucidation of the crystal structure of a Fc-Cε3/Cε4 region of a human IgE was difficult. In one embodiment, crystal structure determination includes obtaining high-resolution data using synchrotron radiation. Such data can be collected, for example, at the Stanford Synchrotron Source Laboratory, Palo Alto, Calif., or the Advanced Photon Source at Argonne National Laboratories, Argonne, Ill. Additional locations to collect such data include, but are not limited to, Brookhaven, N.Y., and Japan. In one embodiment, diffraction data from native and heavy-atom treated crystals provide an initial image of the protein structure which is refined into an electron density map. Details regarding data collection and interpretation are provided in the Examples section.

[0057] One embodiment of the present invention is a method to produce a 3-D model of a Fc region that includes positioning amino acid representations (i.e., representing amino acids) of the protein at substantially the coordinates listed in Table 1, Table 2 or Table 3. That is, knowledge of the coordinates of the complex permits one skilled in the art to produce a model of the protein using those coordinates. Such a model, or any model which is essentially represented by a simple coordinate transformation of the coordinates specified in Table 1, Table 2 or Table 3, can be represented in a variety of methods as heretofore disclosed and is included in the present invention.

[0058] In another embodiment, a model of the present invention can be refined to obtain an improved model, which is an example of a model modification, also referred to as a modified model. Refining methods can include, but are not limited to, further data collection and analysis; data collection from frozen crystals; introduction of solvent molecules to the structure; clarification of secondary structure; and analyses of crystallized complexes between a FcR and an antibody or inhibitory compound or of crystallized FcRs or antibodies alone. An additional model refinement method includes analyzing a 3-D model to predict amino acid residues that if replaced are likely to yield proteins with at least one improved function, effecting at least one such replacement, determining whether the activity of the modified protein agrees with the prediction, and refining the model as necessary. Methods to determine whether the modification agrees with prediction include producing the modified protein and performing assays with that modified protein to determine if the protein does indeed exhibit the improved function(s), such as desired activity, stability and solubility properties. Assays to measure such functions are well known in the art; examples of several such assays are disclosed herein.

[0059] Another embodiment of the present invention is a modified 3-D model that represents an antibody other than human IgE as represented by the coordinates in Table 1, Table 2 or Table 3. Preferably the amino acid sequence of the protein(s) to be modeled is known. In such a case, the modified model can be produced using the technique of homology modeling, preferably by incorporating (e.g., grafting, overlaying or replacing) all or any portion of the amino acid sequence of the other antibody into the 3-D model representing the coordinates of Table 1, Table 2 or Table 3 to produce the modified model. General techniques for homology modeling, also referred to as molecular replacement, have been disclosed in, for example, Greer, 1990, Proteins: Structure, Function, and Genetics 7, 317-334; Havel et al., 1991, J. Mol. Biol. 217, 1-7; Schiffer et al., 1990, Proteins: Structure, Function, and Genetics 8, 30-43; and Lattman, 1985, Methods Enzymol 115, 55-77. However, such technology has not been applied to Fc regions of IgE antibodies since, until the present invention, no 3-D model of any Fc region of IgE was available. Thus, the present invention now allows the solving of the structures of a number of other natural and mutated forms of antibodies.

[0060] In one embodiment, a model of a Fc region, such as, but not limited to a Fc-Cε3/Cε4 region, is produced by extracting the 3-D coordinates from a published figure or building a 3-D model with atoms from other domains wherein FcR-binding domains of the antibody are oriented as predicted for a human Fc-Cε3/Cε4₂₂₂ protein. For example, a model of the present invention can be produced by orienting two known FcR-binding domains into a bent confirmation such that the distance between the domains ranges from about 10 to about 25 angstroms or from about 20 to about 40 angstroms. In another example, a model can be produced by orienting the hinge between two Ig domains in a manner similar to that specified by the coordinates in Table 1, Table 2 or Table 3. Such a model is referred to as a model in which the hinge between two Ig domains, e.g., between Cε3 and Cε4 are oriented in a manner as specified by the structural coordinates listed in Table 1, Table 2 or Table 3. This model can then be used in further molecular replacement methods. Such methods can include the steps of (a) orienting the model by three rotations; and (b) translating the model in one to three directions to produce additional model modifications.

[0061] Suitable antibodies for which a 3-D model can be determined using homology modeling include any mammalian antibody such as a protein that binds to a FcR for IgE, IgG, IgM, IgA or IgD antibodies. Preferred antibodies that bind to FcRs include human, canine, feline, equine, murine and rat antibodies. The present invention also includes the use of other Ig domains to produce models of the present invention.

[0062] One embodiment of the present invention is a 3-D model of a Fc region of an antibody in which the protein has an improved function compared to an unmodified protein as well as a method to produce such a modified model. Such an improved function includes, but is not limited to, enhanced activity, enhanced stability and enhanced solubility. Such a modified model can be produced by replacing at least one amino acid based on information derived from analyzing the 3-D model representing the coordinates in Table 1, Table 2 or Table 3, such that the replacement leads to a protein with an improved function. As used herein, a replacement refers to an (i.e., one or more) amino acid substitution, insertion, deletion, inversion and/or derivatization (e.g., acetylation, glycosylation, phosphorylation, PEG modification, biotinylation, and covalent attachment of other ligands or other compounds to the protein. In one embodiment, synthetic chemical methods are used to produce either a fragment or the entire protein to, for example, introduce non-natural amino acids or other chemical compounds into the structure of a Fc region. For example, based on a structure of the present invention, one can design synthetic peptides or larger proteins that could be linked to produce an intact protein with FcR binding activity, the structure allowing one to design the start and stop points for these peptides, e.g., at surface accessible loops. In accordance with the present invention, an amino acid that is substituted or inserted can be a natural amino acid or an unnatural amino acid, including a derivitized amino acid. Methods to identify regions in the protein that, if changed, yield a protein with an improved function are disclosed below.

[0063] The present invention includes use of a 3-D model of the present invention to identify a compound that inhibits binding between a FcR and an antibody. The advantages of using a 3-D model to identify inhibitory compounds are multi-fold in that the model depicts the site at which a Fc region of an antibody binds to its FcR, i.e., the antibody-binding domain, also referred to as the antibody binding site, and the FcR-binding domain, also referred to as the FcR binding site. The antibody binding site and the FcR binding site together form an FcR:antibody interaction site. As such, a large number of potential inhibitory compounds can be initially analyzed without having to perform in vitro or in vivo laboratory studies. As used herein, methods to identify inhibitory compounds include, but are not limited to, designing inhibitory compounds based on the 3-D model of a Fc region, probing such a 3-D model with compounds that are potential inhibitors in order to identify those compounds that are actually inhibitory of the binding of an antibody to its FcR, screening a compound data base using such a 3-D model to identify compounds that inhibit such binding, and combinations thereof. Methods to use 3-D models to design, probe for, or screen for suitable inhibitory compounds are known to those skilled in the art. In particular, there are a number of computer programs that enable such methods. See, for example, PCT Publication No. WO 95/35367, by Wilson et al., published Dec. 28, 1995, which is incorporated by reference herein in its entirety.

[0064] An inhibitory compound can be any natural or synthetic compound that inhibits the binding of an antibody to a FcR. Examples include, but are not limited to, inorganic compounds, oligonucleotides, proteins, peptides, antibodies, antibody fragments, mimetics of peptides or antibodies (such as, mimetics of antibody or receptor binding sites), and other organic compounds. Compounds can inhibit binding in either a competitive or non-competitive manner and can either interact at the binding site or allosterically. An inhibitory compound should be capable of physically and structurally associating with a FcR and/or an antibody such that the compound can inhibit binding between the two entitites. As such, an inhibitory compound is preferably small and is of a structure that effectively prevents or disrupts binding. Inhibitory compounds can be identified in one or multiple steps. For example, a compound initially identified that inhibits binding between an antibody and FcR to some extent can be used as a lead to design, probe or screen for a compound with improved characteristics, such as greater efficacy, safety, solubility, etc. A preferred inhibitory compound is a compound that is efficacious when administered to an animal in an amount that results in a serum concentration of from about 1 nanomolar (nM) to 100 micromolar (uM), with a concentration of from about 10 nM to 10 uM being more preferred.

[0065] One embodiment of the present invention is a method to identify a compound that inhibits the binding between an IgE antibody and a FcεRIα protein. Such a method includes the step of using a 3-D model substantially representing the atomic coordinates specified in Table 1, Table 2 or Table 3 to identify such a compound. Included in the present invention are inhibitory compounds that interact directly with the IgE binding domain or the receptor binding domain of the IgE antibody as well as compounds that interact indirectly with such structures. Preferably a compound interacts with at least one of the following regions: a FcεRIα binding domain, an interdomain groove between the two Cε3/Cε4 domains of the antibody Fc region, a hinge between Cε3 and Cε4 domains of the antibody Fc region, and a region of a Cε3 or Cε4 domain, the relative position of which changes by greater than 1 angstrom between closed and receptor-bound Fc-Cε3/Cε4 conformations. It is to be noted that many residues in the Cε3 domains are significantly closer to the Cε4 domains in the closed form of the IgE as compared to the open form. While not being bound by theory, it is believed that molecules that could interact with Cε3 residues and Cε4 residues at the same time but only in the closed form of the IgE, would be potential inhibitors. Regions to target include a set of residues in the two domains whose relative distances change significantly (i.e., by more than 1 angstrom) in comparison of the receptor-bound and closed IgE conformations. Preferably the distance between the two Cε3 domains of the closed conformation of the Fc-Cε3/Cε4 region ranges from about 10 to about 25 angstroms, more preferably from about 10 and 15 angstroms, and even more preferably about 13 angstroms. In a preferred embodiment, an inhibitory compound reacts with at least one of the following regions: a linker between Cε2 and Cε3 (amino acids 4, 7, 8, 9, 10 and 11 of SEQ ID NO:2); a BC loop of Cε3 (amino acids 37, 38 and 39 of SEQ ID NO:2; a DE loop of Cε3 (amino acids 68, 69, and 70 of SEQ ID NO:2); a FG loop of Cε3 (amino acids 99, 100, 101 and 102 of SEQ ID NO:2); a loop or strand defining (i.e., abutting, forming) the interdomain groove; a AB helix of Cε3 (amino acid 20, 21, 22, 23 and 24 of SEQ ID NO:2) which is thought to regulate the full conformational flexibility of the IgE-Fc region; and a region lying above said AB helix of Cε3, i.e., the region constituting the hinge and including amino acids 17, 18 and 19 (after strand A), amino acids 29, 30 and 31 (after strand B), and amino acids 109, 110 and 111 (after strand G) of SEQ ID NO:2. Particularly preferred amino acids with which to have an inhibitory compound interact include: (a) a residue at position 4, 7, 8, 9, 10, 11, 17, 18, 19, 20, 21, 22, 23, 24, 29, 30, 31, 37, 38, 39, 68, 69, 70, 99, 100, 101, 102, 109, 110, or 111 of SEQ ID NO:2; and (b) a surface residue within about 10 angstroms of any of said residues of (a). Even more preferred residues include: (a) a residue at position 4, 7, 8, 9, 10, 11, 37, 38, 39, 68, 69, 70, 99, 100, 101, or 102 of SEQ ID NO:2; (b) a residue in a region of a Cε3 or Cε4 domain, the relative position of which changes by greater than 1 angstrom between closed and receptor-bound Fc-Cε3/Cε4 conformations; and (c) a surface residue within about 10 angstroms of any of said residues of (a) or (b). Also preferred are additional residues identified in the Examples as being in at least one of the above cited regions. One preferred embodiment is a compound that inhibits the ability of an IgE antibody to convert from a closed conformation into a receptor-bound or open conformation. It is to be noted that the ability to identify such key regions and residues is only possible in view of a model of the present invention. In one embodiment, an inhibitory compound of the present invention is a peptide corresponding to at least a portion of any of the identified regions or a derivative thereof, such as a peptide mimetic or other compound that mimics that peptide.

[0066] One embodiment of a method to identify a compound that inhibits the binding between an IgE antibody and a FcεRIα protein includes the steps of: (a) generating a model substantially representing the atomic coordinates listed in Table 1, Table 2 or Table 3 or of the binding domains thereof, on a computer screen; (b) generating the spacial structure of a compound to be tested; and (c) testing to determine if the compound interacts with said FcR binding domain, wherein such an interaction indicates that the compound is capable of inhibiting the binding of an IgE antibody to a FcεRIα protein. In a preferred embodiment, step (a) includes the step of identifying one or more amino acid(s) in the FcR binding domain of the model that interact directly with the FcR. Preferably a compound to be tested will interact directly with one or more of those amino acid(s). Preferred amino acids with which an inhibitory compound should interact are disclosed herein.

[0067] The present invention also includes inhibitory compounds isolated in accordance with the methods disclosed herein. Methods to produce such compounds in quantities sufficient for use, for example, as protective agents (e.g., preventatives or therapeutics) are known to those skilled in the art. It should also be appreciated that it is within the scope of the present invention to expand the use of models of the present invention to produce models of any suitable Fc regions (i.e., model modifications) and to identify compounds that inhibit the binding of antibodies to such Fc regions.

[0068] A preferred inhibitory compound of the present invention, or lead that can be used to produce a more efficacious inhibitory compound, is a saturated tetracyclic hydrocarbon perhydrocyclopentanophenanthrene or a derivative thereof. Such a compound can include a structure having the following formula:

[0069] It is to be understood that such a compound can have any number of “R” groups, even though they are not indicated in the formula. Examples of saturated tetracyclic hydrocarbon perhydrocyclopentanophenanthrenes include, but are not limited to, isoprenoids, terpenes, bile acids, detergents (such as CHAPS and CHAPSO) cholestanes, cholic acids, cholesterols, androgens, estrogens, and other steroids. A preferred inhibitory compound, or compound to use as a lead to design a more efficacious compound is 3-[3-(cholamidopropyl) dimethylammonio]-1-propane-sulfonate (CHAPS) or a compound having a similar ring structure. The interaction of CHAPS with amino acids in the FcεRIα protein and Fc-Cε3/Cε4 region is described in further detail in Ser. No. 60/189,853, ibid.

[0070] In one embodiment, an inhibitory compound of the present invention is a bivalent, or other multivalent, compound that interacts with the two Cε3/Cε4 domains with high affinity or a compound that is sufficiently large to bind the interdomain groove, such as, but not limited to, macromolecules such as in vitro selected peptides, peptoids, nucleic acids, similar molecules, mimetopes thereof.

[0071] The present invention also includes use of a 3-D model of the present invention to rationally design and construct modified forms of Fc regions of antibodies, and particularly of IgE antibodies, that have one or more improved functions, such as, but not limited to, increased activity, increased stability and increased solubility compared to an unmodified Fc region of an IgE antibody. Muteins of the present invention include full-length proteins as well as fragments (i.e., truncated versions) of such proteins.

[0072] One embodiment of the present invention is a Fc region that comprises a mutein that binds to a Fc binding domain of a FcR. Such a mutein has an improved function compared to a protein comprising SEQ ID NO:2. Examples of such an improved function include, but are not limited to, increased stability, increased affinity for an FcR, altered substrate specificity, and increased solubility. Such a mutein can be produced by a method that includes the steps of: (a) analyzing a 3-D model substantially representing the atomic coordinates specified in Table 1, Table 2 or Table 3 to identify at least one amino acid of the protein represented by the model which if replaced by a specified amino acid would effect the improved function of the protein; and (b) replacing the identified amino acid(s) to produce a mutein having the improved function. Knowledge of the coordinates allows one to target specific residues, e.g. in the hydrophobic core or on the surface, to generate an accessible set of variants that can then be selected for a particular property, e.g. high stability, high affinity, altered substrate specificity, or other desirable properties (i.e., improved functions). Without the coordinates, one would have to analyze an extraordinarily large number of variants, e.g., on the order of ˜10¹¹ possibilities. The structure, in contrast, allows one to pick the most relevant residues for selecting a desired property by, for example, phage display or other methods. In a preferred embodiment, replacement of one or more amino acids does not substantially disrupt the 3-D structure of the protein; i.e., the modified protein, or mutein, is still capable of binding to the FcR. A preferred mutein is a Fc domain of an IgE antibody that binds to a FcεRIα protein, although the invention also covers muteins binding to other classes of FcRs.

[0073] In one embodiment, a mutein of the present invention has increased stability compared to its unmodified counterpart. As used herein, increased stability refers to the ability of a mutein to be more resistant, for example, to higher or lower temperature, to more acidic or basic pH, to higher or lower salt concentrations, to oxidation and/or reduction, to deamidation, to other forms of chemical degradation and to proteolytic degradation compared to an unmodified Fc region. Increased stability can also refer to the ability of a mutein of the present invention to be stable for a longer period of time either during storage (i.e., to have a longer shelf life) or during use (i.e., to have a longer half-life under reaction conditions) than does an unmodified protein. Muteins of the present invention can also exhibit a decreased entropy of unfolding, thereby stabilizing the proteins. Increased stability can be measured using a variety of methods known to those skilled in the art; examples include, but are not limited to, determination of melting temperature, thermal denaturation, pressure denaturation, enthalpy of unfolding, free energy of the protein, or stability in the presence of a chaotropic agents such as urea, guanidinium chloride, guanidinium thiocyanate, etc. A preferred mutein of the present invention has a melting temperature substantially higher than that of an unmodified Fc region. Preferably the melting temperature of a mutein is at least about 1° C. higher, and more preferably at least about 10° C. higher than the melting temperature of the corresponding unmodified protein. Also preferred is a mutein having binding activity over a pH range that is at least about 1 pH unit higher and/or lower than the active pH range of the corresponding unmodified protein.

[0074] Another embodiment of the present invention is a mutein that exhibits increased affinity for a FcR compared to its unmodified counterpart. As used herein, a mutein having increased affinity is a Fc region that exhibits a higher affinity constant (K_(A)) or lower dissociation constant (K_(D)) than its unmodified counterpart. Such a higher affinity constant can be achieved by increasing the association rate (k_(a)) between the mutein and the FcR and/or decreasing the dissociation rate (k_(d)) between the mutein and the FcR. A preferred mutein of the present invention has a K_(A) for a FcR of at least about 3×10⁹ liters/mole (M⁻¹), which is equivalent to a K_(D) of less than or equal to about 3.3×10⁻¹⁰ moles/liter (M). More preferred is a mutein having a K_(A) for a FcR of at least about 2×10¹⁰ M⁻¹, and even more preferably of at least about 1×10¹¹ M⁻¹. Also preferred is a mutein having a k_(a) for a FcR of at least about 1×10⁵ liters/mole-second as well as a mutein having a k_(d) for a FcR of less than or equal to 3×10⁻⁵/second. More preferred is a mutein having a k_(a) for a FcR of at least about 3×10⁵ liters/mole-second, and even more preferably of 1×10⁶ liters/mole-second. Also preferred are muteins having a k_(d) for a FcR of less than or equal to 1×10⁻⁵/second or even more preferably less than or equal to 3×10⁻⁴/second. A preferred FcR is FcεRIα. Methods to measure such binding constants is well known to those skilled in the art; see, for example, Cook et al., 1997, ibid., which reports the following values for the binding of human FcεRIα protein to human IgE: k_(a1) of 3.5 (±0.9)×10⁵ M⁻¹s⁻¹; k_(a2) of 8.6 (±3.5)×10⁴ M⁻¹s⁻¹; k_(d1) of 1.2 (±0.1)×10⁻² s⁻¹; k_(d2) of 3.2 (±0.8)×10⁻⁵ s⁻¹; K_(A1) of 2.0×10⁷ M⁻¹; K_(A2) of 2.9×10⁹ M⁻¹.

[0075] Another embodiment of the present invention is a mutein that exhibits altered substrate specificity compared to its unmodified counterpart. A mutein exhibiting altered substrate specificity is a mutein that binds with increased affinity to a FcR for an antibody class or antibody species of a different type than that normally bound by its unmodified counterpart. In one embodiment, a mutein of a human Fc-Cε3/Cε4 region with altered substrate specificity is a Fc region that binds with increased affinity to a receptor that binds to an IgE antibody of another mammal, such as, but not limited to, a canine, feline, equine, murine, or rat IgE antibody. In another embodiment, a mutein of a human Fc-Cε3/Cε4 region with altered substrate specificity is a Fc region that binds with increased affinity to a Fc receptor for an antibody of another class, such as IgG, IgM, IgA, or IgD, with IgG being preferred. Such a mutein can also show altered species substrate specificity. Methods to determine whether a mutein exhibits altered substrate specificity are well known to those skilled in the art.

[0076] Yet another embodiment of the present invention is a mutein that exhibits increased solubility compared to its unmodified counterpart. Such a protein is less likely to form aggregates. Methods to determine whether a mutein exhibits increased solubility are well known to those skilled in the art.

[0077] As disclosed herein, the 3-D model substantially representing the coordinates in Table 1, Table 2 or Table 3 is advantageous in determining strategies for producing muteins having an improved function, e.g., for identifying targets to modify in order to obtain muteins having improved functions. Examples of targets include, but are not limited to, those regions of the Fc-Cε3/Cε4 region that directly or indirectly interact with a FcεRIα protein.

[0078] In accordance with the present invention, a mutein having an improved function can be produced by a method that includes replacing at least one amino acid based on information derived from analyzing a 3-D model of the present invention to produce the mutein having the improved function. Knowledge of the structure of the human Fc-Cε3/Cε4 region, for example, permits the rational design and construction of modified forms of the protein by permitting the prediction and production of substitutions, insertions, deletions, inversions and/or derivatizations that effect an improved function. That is, analysis of 3-D models of the present invention provide information as to which amino acid residues are important and, as such, which amino acids can be changed without harming the protein. In making amino acid replacements, it is preferred to use amino acid replacements that have similar numbers of atoms and that allow conservation of salt bridges, hydrophobic interactions and hydrogen bonds unless the goal is to purposefully change such interactions. The 3-D structure of the human Fc-Cε3/Cε4 region suggests that large deletions may not be desirable, particularly due to the relation between the various domains of the protein and the observation that most of the structure is well ordered in the crystal.

[0079] It is to be appreciated that although one amino acid replacement capable of improving the function of a protein can substantially improve that function, more than one amino acid replacement can result in cumulative changes depending on the number and location of the replacements. For example, although one amino acid replacement capable of substantially increasing the stability of a protein can increase the melting temperature of that modified protein by about 1° C, about 5 to about 6 replacements may increase the melting temperature of the resultant protein by about 10° C.

[0080] In accordance with the present invention, the 3-D model of the Fc region has been analyzed, using techniques known to those skilled in the art, to determine the accessibility of the amino acids represented within the model to solvent. Such information is provided in, for example, Table 4 or Table 5.

[0081] A number of methods can be used to produce muteins of the present invention. One method includes the steps of: (a) analyzing a 3-D model substantially representing the coordinates specified in Table 1, Table 2 or Table 3 to identify at least one amino acid of the modeled protein which if replaced by a specified amino acid would effect an improved function; and (b) replacing the identified amino acid(s) to produce a mutein having that improved function. In one embodiment, a method to produce a mutein includes the steps of (a) comparing a key region of a model of a human Fc-Cε3/Cε4 region with the amino acid sequence of a Fc region having an improved function compared to the unmodified Fc-Cε3/Cε4 region in order to identify at least one amino acid segment of the Fc region with the improved function that if incorporated into the Fc-Cε3/Cε4 region represented by the model would give the Fc-Cε3/Cε4 region the improved function; and (b) incorporating the segment into the Fc-Cε3/Cε4 region, thereby providing a mutein with the improved function. In another embodiment, a method to produce a protein includes the steps of: (a) using a model representing a human Fc-Cε3/Cε4 region to identify a 3-D arrangement of residues that can be randomized by mutagenesis to allow the construction of a library of molecules from which a improved function can be selected; and (b) identifying at least one member of the mutagenized library having the improved function. In one example, a mutein is produced by a method that includes the steps of: (a) effecting random mutagenesis of nucleic acid molecules encoding a target of a Fc-Cε3/Cε4 region as identified by analyzing a model of that protein, such as an FcR binding domain; (b) cloning such mutagenized nucleic acid molecules into a phage display library, wherein said phage display library expresses the target; and (c) identifying at least one member of the library that expresses a target with an improved function, such as an FcR binding domain exhibiting increased affinity for an FcR. As stated above, the model allows the use of this technique in a straightforward manner that could not be accomplished in the absence of the model. It is to be also noted that these methods can also be used with other models of the present invention to produce muteins of the present invention.

[0082] The present invention includes a number of methods, based on analysis of a 3-D model of the present invention, to replace (i.e., add, delete, substitute, invert, derivatize) at least one amino acid residue in the protein represented by the model in order to produce a mutein of the present invention. Such methods include, but are not limited to: (a) replacing at least one amino acid in at least one non-constrained loop; (b) joining an amino-terminal amino acid residue to a carboxyl-terminal amino acid residue; (c) replacing at least one amino acid site with an amino acid suitable for derivatization; (d) replacing at least one pair of amino acids of the protein with a cysteine pair to enable the formation of a disulfide bond that stabilizes the protein; (e) replacing at least one amino acid in the FcεRIα binding domain in order to increase the affinity between an IgE Fc region and the corresponding FcR; (f) replacing at least one amino acid of the protein with an amino acid such that the replacement decreases the entropy of unfolding of the protein; (g) replacing at least one asparagine or glutamine of the protein with an amino acid that is less susceptible to deamidation than is the amino acid to be replaced; (h) replacing at least one methionine, histidine or tryptophan with an amino acid that is less susceptible to an oxidation or reduction reaction than is the amino acid to be replaced; (i) replacing at least one arginine of the protein with an amino acid that is less susceptible to dicarbonyl compound modification than is the amino acid to be replaced; (j) replacing at least one amino acid of the protein susceptible to reaction with a reducing sugar sufficient to reduce protein function with an amino acid less susceptible to that reaction; (k) replacing at least one amino acid of the protein with an amino acid capable of increasing the stability of the inner core of the protein; (l) replacing at least one amino acid of the protein with at least one N-linked glycosylation site; (m) replacing at least one N-linked glycosylation site of the protein with at least one amino acid that does not comprise an N-linked glycosylation site; and (n) replacing at least one amino acid of the protein with an amino acid that reduces aggregation of the protein. Muteins of the present invention can be produced using methods and rationales similar to those disclosed in PCT WO 00/26246, ibid.; such methods, which are incorporated herein by reference in their entirety, can be applied to Fc-Cε3/Cε4 muteins of the present invention.

[0083] Amino acid replacements can be carried out using recombinant DNA techniques known to those skilled in the art, including site-directed mutagenesis (e.g., oligonucleotide mutagenesis, random mutagenesis, polymerase chain reaction (PCR)-aided mutagenesis, gapped-circle site-directed mutagenesis) or chemical synthetic methods of a nucleic acid molecule encoding the desired protein, such as, but not limited to a human FcεRIα protein, followed by expression of the mutated gene in a suitable expression system, preferably an insect, mammalian, bacterial, yeast, insect, or mammalian expression system. See, for example, Sambrook et al., ibid.

[0084] It is to be appreciated that muteins of the present invention can include amino acids which are not modified because they would negatively impact the function of the protein. Such amino acids can be identified using a 3-D model of the present invention.

[0085] It should also be appreciated that it is within the scope of the present invention to expand the use of models of the present invention to produce models of and make modifications to any suitable FcRs or other Ig domain-containing proteins to produce muteins having a desired function.

[0086] Antibody muteins have a variety of uses, including but not limited to, diagnostic and therapeutic uses. For example, muteins could be used to image cells that express an antibody receptor protein, such as NMR-specific labeling for in vivo imaging to detect, for example, mast cell cancers, asthma, and other pathologies, or to treat cancers that express an antibody receptor protein using, for example, radioimmune therapy of derivatized IgE. Muteins could also be used for monitoring FcR expression in atopic individuals (e.g. with a tag for one-step FACS analysis) or for monitoring IgE in atopic individuals. Muteins could also be used as inhibitors or as toxin-IgE-Fc fusion proteins to target FcR-expressing cells to kill them (e.g. in mast cell tumors or severe allergy). Also muteins that affect the low affinity affinity IgE-receptor (FceRII) binding but not FceRI binding could be designed or selected.

[0087] The present invention also includes nucleic acid molecules that encode muteins of the present invention as well as recombinant molecules and recombinant cells that include such nucleic acid molecules. Methods to produce such proteins are also disclosed herein.

[0088] The present invention also includes the following novel structures as identified by a 3-D model of the present invention. Preferred structures exhibiting direct interaction between IgE and FcεRIα include a FcεRIα binding domain, an interdomain groove between the two Cε3/Cε4 domains of said antibody Fc region, a hinge between Cε3 and Cε4 domains of said antibody Fc region, and a region of a Cε3 or Cε4 domain, the relative position of which changes by greater than 1 angstrom between closed and receptor-bound Fc-Cε3/Cε4 conformations. Preferred compositions include a linker between Cε2 and Cε3, a BC loop of Cε3, a DE loop of Cε3, and a FG loop of Cε3, a loop or strand defining the interdomain groove, a AB helix of Cε3 and, a region lying above said AB helix of Cε3. The present invention also includes nucleic acid molecules to encode such compositions.

[0089] The present invention also includes an isolated Fc-Cε3/Cε4 protein selected from the group consisting of: (a) a protein consisting of SEQ ID NO:2; and (b) an isolated protein that is structurally homologous to a protein of (a), wherein said protein of (b) binds to a FcεRIα protein. Also included in the present invention is such a protein produced in insect cells. In one embodiment the Fc-Cε3/Cε4 protein a human Fc-Cε3/Cε4 protein, a canine Fc-Cε3/Cε4 protein, a feline Fc-Cε3/Cε4 protein, an equine Fc-Cε3/Cε4 protein, a murine Fc-Cε3/Cε4 protein, or a rat Fc-Cε3/Cε4 protein. The present invention also includes nucleic acid molecules that encode such proteins, as well as recombinant molecules, recombinant cells and recombinant viruses that include such nucleic acid molecules. Also included are methods to produce such proteins using such nucleic acid molecules, recombinant molecules, recombinant viruses and recombinant cells.

[0090] The present invention also includes isolated nucleic acid molecules encoding proteins of the present invention, including, but not limited to, unmodified proteins, novel structures within such proteins, and muteins. As used herein, an isolated nucleic acid molecule encoding a protein is a nucleic acid molecule that has been removed from its natural milieu. As such, “isolated” does not reflect the extent to which the nucleic acid molecule has been purified. An isolated nucleic acid molecule can be DNA, RNA, or derivatives of either DNA or RNA.

[0091] A nucleic acid molecule encoding a mutein of the present invention can be produced by mutation of parental protein genes (e.g., unmodified or previously modified protein-encoding genes, or portions thereof) using recombinant DNA techniques heretofore disclosed or by chemical synthesis. Resultant mutein nucleic acid molecules can be amplified using recombinant DNA techniques known to those skilled in the art, such as PCR amplification or cloning (see, for example, Sambrook et al., ibid.), or by chemical synthesis. A mutein can also be produced by chemical modification of a protein expressed by a nucleic acid molecule encoding an unmodified protein or mutein-encoding gene.

[0092] Proteins of the present invention can be produced in a variety of ways, including production and recovery of recombinant proteins and chemical synthesis. In one embodiment, a protein of the present invention is produced by culturing a cell capable of expressing the protein under conditions effective to produce the protein, and recovering the protein. A preferred cell to culture is a recombinant cell that is capable of expressing the protein, the recombinant cell being produced by transforming a host cell with one or more nucleic acid molecules of the present invention. Transformation of a nucleic acid molecule into a host cell can be accomplished by any method by which a nucleic acid molecule can be inserted into a cell. Transformation techniques include, but are not limited to, transfection, electroporation, microinjection, lipofection, adsorption, and protoplast fusion. A recombinant cell may remain unicellular or may grow into a tissue, organ or a multicellular organism. Transformed nucleic acid molecules of the present invention can remain extrachromosomal or can integrate into one or more sites within a chromosome of a host cell in such a manner that their ability to be expressed is retained.

[0093] Suitable host cells to transform include any cell that can be transformed. Host cells can be either untransformed cells or cells that are already transformed with at least one nucleic acid molecule. Host cells of the present invention can be endogenously (i.e., naturally) capable of producing a protein of the present invention, but such cells are not preferred. Host cells of the present invention can be any cell that when transformed with a nucleic acid molecule of the present invention are capable of producing a protein of the present invention, including bacterial, yeast, other fungal, insect, animal, and plant cells. Preferred host cells include bacterial, yeast, insect and mammalian cells, and more preferred host cells include Escherichia, Bacillus, Saccharomyces, Pichia, Trichoplusia, Spodoptera and mammalian cells. Particularly preferred host cells are Trichoplusia ni cells and Spodoptera frugiperda cells with T. ni cells being particularly preferred.

[0094] A recombinant cell is preferably produced by transforming a host cell with a recombinant molecule comprising a nucleic acid molecule of the present invention operatively linked to an expression vector containing one or more transcription control sequences. The phrase operatively linked refers to insertion of a nucleic acid molecule into an expression vector in a manner such that the molecule is able to be expressed when transformed into a host cell. As used herein, an expression vector is a DNA or RNA vector that is capable of transforming a host cell, of replicating within the host cell, and of effecting expression of a specified nucleic acid molecule. Expression vectors can be either prokaryotic or eukaryotic, and are typically viruses or plasmids. Expression vectors of the present invention include any vectors that function (i.e., direct gene expression) in recombinant cells of the present invention, including in bacterial, yeast, other fungal, insect, animal, and plant cells. Preferred expression vectors of the present invention can direct gene expression in bacterial, yeast, insect and mammalian cells.

[0095] Nucleic acid molecules of the present invention can be operatively linked to expression vectors containing regulatory control sequences such as promoters, operators, repressors, enhancers, termination sequences, origins of replication, and other regulatory control sequences that are compatible with the host cell and that control the expression of the nucleic acid molecules. In particular, recombinant molecules of the present invention include transcription control sequences. Transcription control sequences are sequences which control the initiation, elongation, and termination of transcription. Particularly important transcription control sequences are those which control transcription initiation, such as promoter, enhancer, operator and repressor sequences. Suitable transcription control sequences include any transcription control sequence that can function in at least one of the recombinant cells of the present invention. A variety of such transcription control sequences are known to those skilled in the art. Preferred transcription control sequences include those which function in bacterial, yeast, insect and mammalian cells.

[0096] It may be appreciated by one skilled in the art that use of recombinant DNA technologies can improve expression of transformed nucleic acid molecules by manipulating, for example, the number of copies of the nucleic acid molecules within a host cell, the efficiency with which those nucleic acid molecules are transcribed, the efficiency with which the resultant transcripts are translated, and the efficiency of post-translational modifications. Recombinant techniques useful for increasing the expression of nucleic acid molecules of the present invention include, but are not limited to, operatively linking nucleic acid molecules to high-copy number plasmids, integration of the nucleic acid molecules into one or more host cell chromosomes, addition of vector stability sequences to plasmids, substitutions or modifications of transcription control signals (e.g., promoters, operators, enhancers), substitutions or modifications of translational control signals (e.g., ribosome binding sites, Shine-Dalgarno sequences), modification of nucleic acid molecules of the present invention to correspond to the codon usage of the host cell, deletion of sequences that destabilize transcripts, and use of control signals that temporally separate recombinant cell growth from recombinant protein production during fermentation. The activity of an expressed recombinant protein of the present invention may be improved by fragmenting, modifying, or derivatizing nucleic acid molecules encoding such a protein.

[0097] In accordance with the present invention, recombinant cells can be used to produce proteins by culturing such cells under conditions effective to produce such a protein, and recovering the protein. Effective conditions to produce a protein include, but are not limited to, appropriate media, bioreactor, temperature, pH and oxygen conditions that permit protein production. An appropriate medium refers to any medium in which a cell of the present invention, when cultured, is capable of producing the protein. An effective medium is typically an aqueous medium comprising assimilable carbohydrate, nitrogen and phosphate sources, as well as appropriate salts, minerals, metals and other nutrients, such as vitamins. The medium may comprise complex nutrients or may be a defined minimal medium. Cells of the present invention can be cultured in conventional fermentation bioreactors, which include, but are not limited to, batch, fed-batch, cell recycle, and continuous fermentors. Culturing can also be conducted in shake flasks, test tubes, microtiter dishes, and petri plates. Culturing is carried out at a temperature, pH and oxygen content appropriate for the recombinant cell. Such culturing conditions are well within the expertise of one of ordinary skill in the art.

[0098] Depending on the vector and host system used for production, resultant proteins may either remain within the recombinant cell; be secreted into the fermentation medium; be secreted into a space between two cellular membranes, such as the periplasmic space in E. coli; or be retained on the outer surface of a cell or viral membrane. The phrase “recovering the protein” refers simply to collecting the whole fermentation medium containing the protein and need not imply additional steps of separation or purification. Proteins of the present invention can be purified using a variety of standard protein purification techniques, such as, but not limited to, affinity chromatography, ion exchange chromatography, filtration, electrophoresis, hydrophobic interaction chromatography, gel filtration chromatography, reverse phase chromatography, chromatofocusing and differential solubilization.

[0099] The present invention also includes isolated (i.e., removed from their natural milieu) antibodies that selectively bind to a Fc region of the present invention. As used herein, the term “selectively binds to” refers to the ability of antibodies of the present invention to preferentially bind to an Fc region of the present invention. Binding can be measured using a variety of methods standard in the art including enzyme immunoassays (e.g., ELISA), immunoblot assays, etc.; see, for example, Sambrook et al., ibid. Isolated antibodies of the present invention can include antibodies in a bodily fluid (such as, but not limited to, serum), or antibodies that have been purified to varying degrees. Antibodies of the present invention can be polyclonal or monoclonal. Functional equivalents of such antibodies, such as antibody fragments and genetically-engineered antibodies (including single chain antibodies or chimeric antibodies that can bind to more than one epitope) are also included in the present invention. Antibodies can be produced using methods known to those skilled in the art. A preferred method to produce antibodies of the present invention includes (a) administering to an animal an effective amount of a protein of the present invention to produce the antibodies and (b) recovering the antibodies. In another method, antibodies of the present invention are produced recombinantly using techniques as heretofore disclosed to produce proteins of the present invention. Antibodies raised against defined proteins can be advantageous because such antibodies are not substantially contaminated with antibodies against other substances that might otherwise cause interference in a diagnostic assay or side effects if used in a therapeutic composition.

[0100] Antibodies of the present invention have a variety of potential uses that are within the scope of the present invention. Examples of such uses are disclosed in WO 98/27208, ibid., see, for example, page 24; such uses are incorporated by reference herein in their entireties.

[0101] A Fc region of the present invention can include chimeric molecules comprising at least a portion of a Fc region that binds to an antibody and a second molecule that enables the chimeric molecule to be bound to a substrate in such a manner that the antibody receptor portion binds to the antibody in at least as effective a manner as a Fc region that is not bound to a substrate. An example of a suitable second molecule includes a portion of an immunoglobulin molecule or another ligand that has a suitable binding partner that can be immobilized on a substrate, e.g., biotin and avidin, or a metal-binding protein and a metal (e.g., His), or a sugar-binding protein and a sugar (e.g., maltose).

[0102] The present invention includes uses of Fc regions, antibodies thereto, and inhibitory compounds of the present invention for the diagnosis and treatment of allergy and the regulation of other immune responses in an animal.

[0103] One embodiment is a therapeutic composition comprising at least one of the following therapeutic compounds: an inhibitory compound of the present invention, a mutein of the present invention, or an antibody of the present invention. Also included is a method to protect an animal from allergy or other abnormal immune responses. Such a method includes the step of administering a therapeutic composition of the present invention to the animal. As used herein, the ability of a therapeutic composition of the present invention to protect an animal from allergy or other abnormal immune responses refers to the ability of that composition to, for example, treat, ameliorate or prevent allergy or other abnormal immune responses. General characteristics of therapeutic compositions and methods to produce and use such therapeutic compositions are disclosed, for example, in WO 98/27208, ibid., see, for example, page 39-47; such compositions and methods are incorporated by reference herein in their entireties. It is to be noted that although the compositions and methods disclosed in WO 98/27208, ibid., relate to feline FcεRIα proteins, they are also applicable to therapeutic compositions of the present invention. Therapeutic compositions of the present invention are advantageous because they can be derived from analysis of 3-D models of the present invention and have improved functions, such as efficacy and safety.

[0104] Another embodiment is a diagnostic reagent comprising a mutein of the present invention. As used herein, a diagnostic reagent is a composition that includes a mutein that is used to detect allergy or other abnormal immune responses in an animal. Also included in the present invention are methods, including in vivo methods and in vitro methods, to (a) detect allergy or other abnormal immune response, or susceptibility thereto, in an animal, comprising use of a diagnostic reagent comprising a mutein of the present invention and (b) to enhance the performance of an IgE or FcR binding assay, said method comprising incorporating into the assay a mutein of the present invention. General characteristics of diagnostic reagents and methods to produce and use such diagnostic reagents are disclosed, for example, in WO 98/27208, ibid., see, for example, page 2-39; such reagents and methods are incorporated by reference herein in their entireties. It is to be noted that although the reagents and methods disclosed in WO 98/27208, ibid., relate to feline FcεRIα proteins, they are also applicable to diagnostic reagents, kits and detection methods of the present invention. Muteins of the present invention are advantageous in such applications because of their enhanced affinity for antibodies, altered specificity, enhanced solubility and/or enhanced stability, enabling for example use in otherwise adverse conditions and longer shelf-life.

[0105] The following examples are provided for the purposes of illustration and are not intended to limit the scope of the invention.

EXAMPLES Example 1

[0106] This Example describes the production and analysis of a crystal and model of the present invention. It is to be noted that numbering of Fc-Ce3/Ce4 residues follows the convention of Dorrington et al, ibid.

[0107] The binding of soluble IgE to its high affinity receptor, FcεRI, is a requisite step in the cascade of events associated with the allergic response and anti-parasitic immunity¹⁻³. Crosslinking of receptor-bound IgE by antigens triggers intracellular signaling events leading to effector cell activation⁴. This example describes the solution of a 2.3 Å crystal structure of the human IgE-Fc domains, Cε3 and Cε4, which bind to FcεRI, the coordinates of which are disclosed in Table 1. The IgE-Fc crystal structure reveals a large (˜15•) tertiary rearrangement of the Cε3 domains when compared to IgG-Fc structures and the IgE-Fc bound to FcεRI. The free IgE-Fc adopts a more compact arrangement that places the Cε3 domains into close proximity in a “closed” configuration, obstructing receptor-binding loops. This IgE-Fc conformational change is mediated by three flexible segments that lie within the Cε3 domain and not by the interdomain connecting loop. The “closed” structure of the IgE-Fc highlights the potential for novel conformational variation in the effector domains of different antibody classes and suggests new strategies for the design of therapeutic compounds for the treatment of allergy and asthma.

[0108] The interaction of antibody Fc domains with cellular antibody receptors couples the diversity of the antibody repertoire to many effector cells of the immune system. Fc receptors specific for antibody subclasses, including IgE, IgG and IgA antibodies, are found on overlapping but distinct subsets of cells of the hematopoetic system and can thereby trigger distinct mechanisms of the immune response^(1,4,5). IgE-mediated immune reactions are implicated in parasitic infections, allergy and asthma.

[0109] IgE antibodies consist of two Fabs and an Fc that is formed by a dimer of three constant domains (Cε2, Cε3, and Cε4). Compared to IgG molecules, IgE has an additional constant domain (Cε2) that replaces the IgG linker region, while the IgE Cε3 and Cε4 domains are homologous to the IgG Cγ2 and Cγ3 domains. Intact IgE and Fc fragments bind with high affinity (K_(D)˜10⁻⁹-10⁻¹⁰ M) to the alpha chain of FcεRI and mutagenesis studies⁶⁻¹¹ have demonstrated that Cε3 domain residues are involved in binding to the receptor, consistent with the crystallographic studies of the IgE-Fc:FcεRIα complex. The IgE-Cε2 domains are not thought to be important for receptor binding, since constructs of the IgE-Cε3/Cε4 domains retain high affinity binding to the receptor.

[0110] In order to obtain protein for crystallographic studies, the C-terminal IgE-Fc domains, Cε3/Cε4, were expressed in insect cells and purified as described in the methods section. Crystals were obtained that diffract weakly using laboratory X-ray sources but diffract to 2.3 Å using high energy synchrotron X-ray sources. The IgE-Fc Cε3/Cε4 structure was solved by an automated molecular replacement search strategy using ˜12,000 distinct conformational variants of core models for the two immunoglobulin domains, in which the domain orientations were varied by rotation about three axes centered near the connecting loop between the two domains. A course (3• angular) search yielded a single promising solution that was further refined by finer domain rotations. The structure was subjected to rounds of refinement and building into simulated annealing composite omit electron density maps, giving the final statistics shown in Table 6. The Rfree and Rfactor are, respectively, with good geometry to 2.3 Å resolution.

[0111] The overall structure for the IgE Cε3/Cε4 domains is shown in FIGS. 1a and 2 a. The two immunoglobulin domains belong to the C1 set of antibody constant domains and are individually similar to the structures for the receptor-bound IgE-Fc and IgG-Fc domains shown in FIGS. 1b, 2 b and 1 c, 2 c, respectively. No density for residues N-terminal to V336 (the Cε2/Cε3 linker) are observed in the IgE-Fc structure, despite the fact that an interchain disulfide occurs in this region and can be shown to form biochemically. The Cε2/Cε3 linker becomes ordered and visible in electron-density maps upon binding FcεRI (see, for example, Ser. No. 60/189,853). Similar to the IgG-Fc, the Cε3 domains of the heavy chain dimer do not form any inter-chain contacts, while the Cε4 domains form an extensive dimer interface, burying ˜1860 Å² of surface area. Conserved carbohydrate found at N394 in IgE, fills the cavity between the Cε3 and Cε4 domains and makes limited contacts across the dimer interface. In contrast to IgG-Fc structures; IgE carbohydrate can be removed and binding to FcεRI is retained⁸.

[0112] The IgE-Fc crystal structure reveals a novel and compact closed conformation for the Fc domains. The relative dispositions of the two Cε3 domains with respect to each other and to the Cε4 domains is substantially different from IgG-Fc or the receptor-bound IgE-Fc structures (FIG. 1). The Cε3/Cε4 angle is more acute than that found between IgG-Fc Cγ2/Cγ3 domains or for the receptor-bound IgE-Fc (FIG. 1). The free IgE-Fc is more compact, as shown by its shorter overall height (FIG. 1a, ˜7 Å), with overall dimensions of 58×63×40 Å as compared to 65×64×36 Å for IgG-Fc (FIG. 1c) and to the dimensions of the receptor-bound IgE-Fc (FIG. 1b) (see, for example, Ser. No. 60/189,853). The Cε3 domains in the IgE-Fc structure also approach each other more closely, as shown by the distances between loop residues indicated in FIG. 2a. The distances between the first residue in strand A of the Cε3 or Cγ2 Ig domains can be readily compared, minimizing differences in distance due to loop flexibility. In IgG (FIG. 2c), this distance is ˜22 Å (varies some between IgG structures), in the receptor-bound IgE-Fc (FIG. 2b) this distance is ˜23 Å, while in the closed IgE (FIG. 2a) this distance is ˜13 Å. Overall, the receptor-bound IgE and IgG-Fc structures more closely resemble each other than the unbound IgE-Fc structure.

[0113] Although conformational differences in IgG-Fc structures have been noted^(12,13), these are not as large as observed for the receptor-bound and closed IgE-Fc structures. FIG. 3 shows a superposition of nine different IgG structures along with the closed IgE-Fc structure observed here. The IgE-Fc lies significantly beyond the observed range of motion in IgG-Fc structures. A superposition of the receptor-bound and closed forms of the IgE-Fc is shown in FIG. 3, demonstrating the large conformational change observed. The AB helix of Cε3 and the interdomain linker residues remain relatively fixed with respect to the Cε4 domain, as shown by a superposition of the open and closed IgE conformations (FIG. 3). The largest IgG-Fc conformational differences are found in comparisons of human and mouse IgG-Fc structures that are 65% identical in sequence¹², potentially accounting for some of the conformational differences. In contrast, the IgE-Fc structures compared here demonstrate large conformational flexibility for a molecule of identical sequence.

[0114] An analysis of the IgE-Fc conformational difference is shown in FIG. 4a, in which comparison of the closed and open forms was carried out with the program DynDom¹⁴. Dyndom groups residues that move as semi-rigid domains for proteins in different conformational states and identifies an interdomain screw axis and hinge residues for the IgE domain motion. The axis of the IgE bending motion is indicated by the arrow in FIG. 4a, with an approximately 15• rotation and 0.6 Å translation relating the open and closed forms. The bend between the two domains does not occur in the interdomain region (residues 436-440) but rather occurs within the Cε3 domain itself. The residues that constitute the hinge lie above the Cε3-AB helix and include amino acids 342-344 (after strand A), 354-356 (before strand B), and 434-436 (after strand G) and are highlighted with light purple in FIG. 4a.

[0115] The structural basis for the difference in apparent flexibility in the IgG- and IgE-Fc domains is not simply based on sequence differences in the linker amino acids between the two immunoglobulin domains, given the potential for hinge motion in the three peptide segments identified by DynDom. The interdomain linker region and the AB helix remain relatively fixed in the comparison of closed and open IgE-Fc structures (FIGS. 1c and 4 a). At the C-terminal end of the AB helix, small structural changes account for a single residue insertion in IgG-Cγ2 sequences compared to IgE-Cε3 and these are not part of the hinge regions in IgE (FIG. 4b). In both IgE and IgG, the A and B β-strands of Cε3 or Cγ2 separate and do not hydrogen bond on either side of the AB helix, and it is in this region that the IgE bending appears to concentrate (FIGS. 4a and 4 b). Comparison of the IgG-Fc and IgE-Fc structures shows a concerted shift in the position of the IgE-Fc AB helix outwards from the Cε3/Cε4 interface, which may account for the greater rotational freedom in the IgE-Fc structures (FIG. 4b). In the closed IgE-Fc structure, the hinge residues immediately after the AB helix (amino acids 354-356) sterically clash with the superimposed IgG-Fc AB helix (FIG. 4b). Thus the closed conformation observed here for the IgE-Fc may be inaccessible to the IgG-Fc, because of the position of the IgG-Fc AB helix. Additional residues may also contribute to the conformational differences in IgG and IgE, such as the change of P257/P258 in IgG for R342/P343 in IgE in the A strand and the presence of P354 at the beginning of the IgE-AB helix. Differences in the phi/psi angles accessible to the double proline sequence in IgG could additionally stabilize the open configuration of IgG-Fcs. In contrast to human IgE-Fc, the mouse and rat sequences contain this double proline motif. It will be interesting to test if mutation of R342 for proline stabilizes the open conformation as measured by solution techniques and if this mutation has an effect on the binding affinity for IgE receptors.

[0116] The large conformational change observed in the closed IgE-Fc structure reorients loops at the top of the Cε3 domains that interact with FcεRI. FIG. 4c quantifies these conformational differences by comparing the distance between pairs of Cα carbon atoms in the free IgE-Fc and the receptor-bound IgE-Fc. Loops that are involved in binding FcεRI are highlighted above the graph and these regions are observed to move by 10-14 Å between the bound and free forms of the IgE-Fc. Since the rotation axis lies near the base of the Cε3 domain (FIG. 4a), a gradient of increasing Cα displacements can be seen in this plot that corresponds to amino acids in the Cε3 beta strands. The peaks in the plot correspond to loops at the top of the Cε3 domain that show the largest displacements (FIG. 4c). The AB-helix in the Cε3 domain appears to be linked structurally to the Cε4 domains by this analysis as well as the domain-movements shown in FIG. 3.

[0117] The movement of the IgE-Fc receptor-binding loops by 10-14 Å suggests that these loops would be poorly positioned in the “closed” form to interact with the receptor-binding surface. FIGS. 5a and 5 b show surface representations of the FcR-binding loops of the Cε3 domain for the bound and free forms. The rotation of the Cε3 domains about this internal hinge reorients the receptor-binding surfaces. In the open, receptor-binding form, the Cε3 loops are exposed and together with the N-terminal linker residues to the Cε2 domains, form a crown-like structure that interacts with the broad and convex surface of FcεRI. In contrast, in the closed Fc conformation, the receptor-binding loops are reoriented to point towards each other across the IgE-Fc diad axis, forming a narrower inter-domain gap that cannot accommodate the binding of the receptor. The relatively large space separating Cγ2 domains in IgG and in the Cε3 domains of “open” form of IgE, becomes more of a cleft in the closed IgE-Fc (FIG. 5a).

[0118] The IgE-Fc conformation in solution is likely to be dynamic and the full range of Cε3 conformational mobility remains to be established. However, biophysical studies of IgE conformation in solution have previously suggested more compact models for the IgE conformation as compared to IgG antibodies. Neutron scattering studies of a three domain construct of the IgE-Fc (Cε2/Cε3/Cε4) are consistent with a more compact structure than that of IgG-Fc in solution¹⁵. In addition, N-terminal to C-terminal distances for intact IgE have also been measured by fluorescence energy transfer (˜71 Å) and suggest a bent conformation for the antibody in solution, with less hinge-mediated flexibility as compared to IgG^(16,17). These studies may also be consistent with the more compact IgE-Fc conformation observed in the crystal structure reported here.

[0119] The observed conformational flexibility in the IgE-Fc may be important for unique aspects of IgE biological function. IgE-Fc flexibility may allow for induced-fit interactions with the FcεRI, contributing to the high affinity binding or may also be important in interactions with the low affinity IgE receptor, FcεRII (FIG. 6). FcεRII is a trimeric C-type lectin that is thought to interact with the IgE-Fc through two of the three lectin domains¹⁸. IgG antibodies do not interact with a corresponding lectin-like receptor, consistent with a potential biological role for IgE-Fc conformational variation in this unique antibody-receptor interaction. Finally, the observation of the closed IgE-Fc conformation provides a template for the design of new inhibitors of the IgE-FcεRI interaction (FIG. 6). Stabilization of the closed IgE-Fc conformation by the binding of small molecules, either at directly competitive or indirect allosteric sites, could block receptor association (FIG. 6), leading to a new class of therapeutic inhibitors for the treatment of IgE-mediated allergic diseases. The recent observation that in vitro selected peptides bind to the hinge region of the IgG-Fc, suggests the design of peptides that bind selectively to the closed IgE-Fc hinge to block FcεRI binding¹⁹.

[0120] Methods

[0121] Expression and Crystallization of the Human IgE-Fc

[0122] The IgE-Fc Cε3/Cε4 was expressed in insect cells using the Pharmingen baculogold expression system. Briefly, DNA encoding the Cε3/Cε4 domains were subcloned into the pACgp67 expression vector and recombinant virus generated by established methods. IgE-Fc Cε3/Cε4 protein expression was monitored by a receptor-based ELISA assay and protein was purified by conventional techniques (ion exchange, gel filtration and hydroxyapatite chromatography) from 10-20 liters of supernatants of infected T. ni cells. The Fc construct codes for an N-terminal sequence (ADPCDSN) that includes four amino acids (ADPC) upstream of the native sequence beginning with residue D330. The cysteine is displaced by one residue from the natural IgE-Fc cys328, but forms intramolecular disulfide binds in >95% of the isolated IgE-Fc.

[0123] Purified IgE-Fc was concentrated to 10 mg/ml in 10 mM Tris, pH 8.0, using an e280 nm of 1.32 cm−1 (mg/mL)−1. Crystals were obtained using the hanging drop method by mixing 0.5 ml protein +0.5 ml of precipitant (25 mM Sodium Acetate, pH 4.6, 33% (w/v) polyethylene glycol 4000). Crystals grew at room temperature in 1-3 days and were sensitive to small changes in salt or PEG concentration as well as temperature. Crystals were harvested into 25 mM Sodium Acetate, pH 4.6, 37% PEG 4000 and transferred to a cryoprotectant solution (harvest buffer plus 15% (v/v) ethylene glycol) for ˜30 seconds prior to flash-freezing in liquid nitrogen. Crystals belong to the space group P42₁2 with cell dimensions of a=b=105.6 Å, c=47.1 Å and α=β=γ=90• and contain one Cε3/Cε4 chain per asymmetric unit of the crystal.

[0124] Crystal Structure Determination and Refinement

[0125] Data from the IgE-Fc crystals was initially variably anisotropic, but improved substantially when crystals were treated with heavy atoms used for derivative screening, including platinum, mercury and other metals. Based on these onservations, crystals were treated with 1 mM copper (II) chloride prior to freezing and data collection. Although initial diffraction from native crystals was limited to ˜3.0 Å resolution and often exhibited split lattices, copper-treated crystals diffracted to at least 2.3 Å resolution, with little anisotropy lattice problems. This improvement may be due to the oxidation of residual free cysteines (<5%) in the IgE-Fc N-terminal residues prior to freezing. Data were collected from these crsytals at SSRL beamline 7-1 using a Mar300 imaging plate system and at the Advanced Photon Source DND-CAT 5Idbeamline, using a MarCCD detector. Native and derivative data were processed and integrated using the HKL suite of programs.

[0126] Initial attempts at solving the crystal structure by Molecular Replacement (MR) methods failed, using a variety of models of IgE based on IgG-Fc structures, including individual Ig domains and superpositions of IgG Fc structures among others. MR searches were carried out with Amore, CNS/XPLOR and EPMR without success. Heavy atom searches were carried out with a wide range of compounds (27), concentrations (0.1-20 mM) and pH ranges (4.6-8.5) but did not yield a well-behaved isomorphous derivative.

[0127] Since it was possible that the MR searches failed because of an altered conformation for the IgE-Fc as compared to the search model, a systematic exploration of the bend, twist and Cε3 rotation angles relative to Cε4 was undertaken. For this search, the Cγ2 and Cγ3 domains from the crystal structure of an intact mouse monoclonal antibody (PDB code 1IGT)²⁰ were used that were truncated to exclude non-homologous loops and side-chains, providing a model with 144 residues for 222 in the IgE-Fc construct. The two domains were translated to place the Cγ2/Cγ3 linker residues at the origin, with Cγ2 and Cγ3 oriented to allow a bending rotation to occur about the z-axis. Three rotations around X, Y and Z were applied to the Cγ2 domain, while leaving the Cγ3 fixed, using the program lsqkab from the CCP4 suite²¹. Approximately 12000 models were generated automatically and used in complete Molecular Replacement searches with the program Amore²¹, taking ˜10 days on 5 Silicon Graphics computers. The models covered an angular range of −30 to +40 degrees around the starting model with 3• increments in each rotation. A promising initial search solution was refined by restricting the search range and reducing the rotational stepsize to 0.5 degree increments. This fine search produced a model with a correlation coefficient of 38% and an Rfactor of 489% with data from 15-4 Å resolution. This model was subjected to rigid body refinement and a simulated annealing composite omit map was calculated to 3 Å resolution using the program CNS²². Interpretable density was observed in regions omitted from the search model and errors in the model could be easily identified. Model building and refinement were continued using the programs O²³ and CNS²². The current refinement statistics for all data from 0-2.3 Å resolution are collected in Table 6. TABLE 6 Data Collection and Refinement Data collection: crystal (pH of harvest buffer) (pH 7.5) wtcu3 (pH 6.5) wtcu1 Source APS, DND-CAT SSRL, 7-1 (line = ?) Wavelength, 0.906 Å, 13.67 keV 1.08 Å, 11.48 keV energy Resolution 2.30 Å 2.60 Å (2.38-2.30 Å)† (2.69-2.60 Å)† Completeness 99.8% (99.5%)† 99.9% (99.0%)† Total number 106,855 83,604 of reflections Unique 12,340 8,586 reflections Mosaicity 0.48° 0.65° R_(merge) 5.4% (25.7%)† 6.6% (24.5%)† Average 8.66 (>7.1)† 9.74 (>7.4)† redundancy <I/σI> 33.9 (10.6)† 13.9 (8.6)†

[0128] References

[0129] 1. Kinet, Annu Rev Immunol 17, 931-972 (1999).

[0130] 2. Metzger, Immunol Rev 125, 37-48 (1992).

[0131] 3. Sutton et al., Nature 366, 421-428 (1993).

[0132] 4. Daeron, Annu Rev Immunol 15, 203-234 (1997).

[0133] 5. Ravetch et al., Annu Rev Immunol 16, 421-432 (1998).

[0134] 6. Weetall et al., Immunol 145, 3849-3854 (1990).

[0135] 7. Nissim et al., Embo J 10, 101-107 (1991).

[0136] 8. Basu et al., J Biol Chem 268, 13118-13127 (1993).

[0137] 9. Henry et al., Biochemistry 36, 15568-15578 (1997).

[0138] 10. Presta et al., J Biol Chem 269, 26368-26373 (1994).

[0139] 11. Sayers et al., Biochemistry 37, 16152-16164 (1998).

[0140] 12. Harris et al., J Mol Biol 275, 861-872 (1998).

[0141] 13. Harris. et al., Adv Immunol 72, 191-208 (1999).

[0142] 14. Hayward et al., Proteins 30, 144-154 (1998).

[0143] 15. Beavil et al., Biochemistry 34, 14449-14461 (1995).

[0144] 16. Zheng et al., Biochemistry 30, 9125-9132 (1991).

[0145] 17. Zheng et al., Biochemistry 31, 7446-7456 (1992).

[0146] 18. Shi et al., Biochemistry 36, 2112-2122 (1997).

[0147] 19. DeLano et al., Science 287, 1279-1283 (2000).

[0148] 20. Harris et al., Nature 360, 369-372 (1992).

[0149] 21. Collaborative Computational Project, Acta Cryst. D50, 760-763 (1994).

[0150] 22. Brunger et al., Acta Crystallogr D Biol Crystallogr 54, 905-921 (1998).

[0151] 23. Jones et al., Acta Crystallogr A 47, 110-119 (1991).

Example 2

[0152] This Example describes the further refinement of the model described in Example 1. It is to be noted that numbering of Fc-Cε3/Cε4 (also referred to herein as Fc Cε3-Cε4) residues follows the convention of Dorrington et al, ibid.

[0153] IgE antibodies mediate anti-parasitic immune responses and the inflammatory reactions of allergy and asthma. This Example describes the solution of a crystal structure of the human IgE-Fc Cε3-Cε4 domains to 2.3 Å resolution, the coordinates of which are disclosed in Table 2 and Table 3. The IgE-Fc crystal structure reveals a novel, closed conformation for Fc domains. For example, the structure reveals a large rearrangement of the N-terminal Cε3 domains when compared to related IgG-Fc structures and to the IgE-Fc bound to its high affinity receptor, FcεRI. The IgE-Fc adopts a more compact, closed configuration that places the two Cε3 domains in close proximity, decreases the size of the interdomain cavity and obscures part of the FcεRI-binding site. Unique structural features of the Cε3-Cε4 interdomain interfaces are identified that may enable this conformational flexibility. Fc domain flexibility may allow IgE to form optimal interactions with both of its receptors, FcεRI and FcεRII. The structure of the IgE-Fc suggests new strategies for anti-allergy treatments including the design of molecules that act allosterically to block receptor binding.

[0154] A. Background

[0155] The functional diversity of the antibody repertoire involves both the creation of antigen-specific binding sites and the coupling of these specific binding sites to different effector mechanisms of the immune system. Within the antibody, these two functional roles are found on separable parts of the protein, the Fab and Fc regions. Two antigen-binding sites are contained within the Fab regions of antibodies, which are covalently linked through the antibody heavy chain to Fc effector domains (Harris et al., 1999; Padlan, 1994). The Fc domains provide specificity for the activation of downstream effector functions and are derived solely from constant domains of the antibody heavy chain. Isotype switching during B cell development produces immunoglobulins with identical antigenic specificity connected to different heavy chain constant regions that fall into five major classes or isotypes: IgA, IgD, IgE, IgG and IgM. Different Fc isotypes interact with distinct sets of cellular receptors or soluble proteins to initiate specific defense mechanisms. Effector mechanisms are adapted for specific pathogens, for the physical location of an infection and for different stages of the immune response. Fc-associated effector mechanisms include phagocytosis, the initiation of cellular cytotoxicity and inflammation pathways, the activation of complement and the feedback regulation of antibody production (Daeron, 1997; Kinet, 1999; Ravetch and Clynes, 1998).

[0156] IgE antibodies interact through their Fc domains with two cellular receptors of the immune system, FcεRI and FcεRII (CD23). IgE antibodies bind to the high affinity receptor, FcεRI, on the surface of mast cells, basophils and eosinophils (Kinet, 1999; Metzger, 1992). Binding of polyvalent antigen by the receptor-bound IgE causes receptor aggregation, triggering cellular activation. On mast cells this leads to the release of histamine, inflammatory mediators and vasodilators. Mast cell reactions to environmental allergens are associated with the pathologies of allergy, asthma and anaphylaxis (Turner and Kinet, 1999). Activation of eosinophils by FcεRI provides defense mechanisms against parasitic infection (Gounni et al., 1994; Kinet, 1999), while FcεRI on dendritic cells can deliver IgE-bound antigen into the MHC class II antigen-presentation pathway (Maurer et al., 1998). IgE antibodies also interact with a lower affinity receptor, FcεRII, involved in antigen presentation, cellular cytotoxicity and the regulation of IgE production (Sutton and Gould, 1993). While FcεRI is homologous to a family of antibody receptors specific for IgE, IgG and IgA antibodies, FcεRII belongs to a different structural class of proteins and is uniquely associated with the IgE system.

[0157] IgE is the target of recent therapeutic approaches for asthma using humanized anti-IgE monoclonal antibodies (Chang, 2000; Jardieu and Fick, 1999). Antibodies directed against the IgE-Fc block receptor binding, leading to a decrease in receptor activation and expression levels and triggering a decrease in IgE serum levels. Structural studies of the IgE-Fc may provide new routes to improving anti-IgE therapies and to designing inhibitors for the treatment of a wide variety of atopic diseases.

[0158] IgE contains two antibody light chains associated with two heavy chains of the ε isotype. The three C-terminal constant domains of the heavy chain (Cε2, Cε3 and Cε4) dimerize to form the Fc effector domains. Compared to IgG, IgE antibodies have an additional constant domain, Cε2 (FIG. 7a). The Cε3 and Cε4 domains are homologous to the IgG-Fc Cγ2 and Cγ3 domains, respectively, with 32% sequence identity between human IgE and IgG1 (FIG. 7b). Both intact IgE and IgE-Fc fragments (Cε2-Cε4, Cε3-Cε4) bind with high affinity (K_(D) ˜10⁻⁹-10⁻¹⁰ M) to FcεRI and mutagenesis studies have implicated Cε3-domain residues in mediating this interaction (Basu et al., 1993; Henry et al., 1997; Nissim et al., 1991; Presta et al., 1994; Weetall et al., 1990), as well as the binding to FcεRII (Shi et al., 1997; Sutton and Gould, 1993). IgE-Fc Cε3-Cε4 retains binding to both FcεRI (Basu et al., 1993; Henry et al., 1997; Young et al., 1995) and FcεRII (Shi et al., 1997), suggesting a minimal construct for structural studies.

[0159] Crystallographic studies of antibody Fc domains have previously been limited to the IgG class, leaving open many questions regarding the role of sequence and structural diversity in Fc-effector functions.

[0160] B. Structure Determination

[0161] The C-terminal domains of human IgE-Fc, Cε3-Cε4 (FIG. 7), were expressed in insect cells as described in Methods. The IgE-Fc Cε3-Cε4 protein contains three potential N-linked carbohydrate attachment sites, but only two are glycosylated in vivo, N371 and N394 (Basu et al., 1993; Young et al., 1995). Characterization of the Fc carbohydrate by endoglycosidase digestion, mass spectroscopy of tryptic peptides, and mutational analysis shows that high-mannose carbohydrate is attached to N394, which is a conserved glycosylation site in Fc domains. Although both deglycosylated IgE-Fc (Basu et al., 1993) and high-mannose IgE (Granato and Neeser, 1987) retain high binding affinity for FcεRI, deglycosylated IgE-Fc has a tendency to aggregate, making it a poor candidate for crystallographic studies (Basu et al., 1993).

[0162] The IgE-Fc was purified to homogeneity and crystallized. Crystals belong to space group P42₁2 with cell dimensions a=b=105.6 Å, c=47.1 Å. The crystals contain a single IgE-Fc chain (half of the dimeric molecule) in the asymmetric unit, with the molecular dimer axis lying along a crystallographic dyad. The crystals diffract X-rays to 2.0 Å using synchrotron X-ray sources. Molecular replacement searches using a variety of IgG-Fc models were unsuccessful, as were heavy atom searches. The IgE-Fc Cε3-Cε4 structure was solved by an automated molecular replacement search using ˜12,000 distinct conformational variants of core models for the two Ig domains, systematically varying the angles relating the Cε3 and Cε4 domain models. Data collection and refinement statistics are shown in Table 7. The current R_(free) and R_(work) are 27.0% and 24.2%, respectively, to 2.3 Å resolution. There is no density for the ten amino-terminal residues of the protein (including the interchain disulfide) and the four C-terminal residues. In addition, the density for the Cε4 AB loop is poor. TABLE 7 Data Collection and Refinement Data Collection Statistics Data Set wtcu3 (pH 6.5) wtcu1 (pH 7.5) Source APS DND 5-ID SSRL 7-1 Wavelength 0.906 1.08 (Å) Resolution 30.0-2.30 30.0-2.60 (Å) (2.38-2.30) ^(†) (2.69-2.60)^(†) Completeness 99.8% (99.5%)^(†) 99.9% (99.0%)^(†) Unique 12,340 (106,855) 8,586 (83,604) reflections (Total) Average 8.7 (>7.1)^(†) 9.7 (>7.4)^(†) redundancy <I/σ_(I)> 33.9 (10.6)^(†) 13.9 (8.6)^(†) R_(merge) 5.4% (25.7%)^(†) 6.6% (24.5%)^(†) Refinement (wtcu3): Reflections, 11053 (1269) work (free) Atoms Protein Water R_(work)/R_(free) (Total) Atoms Molecules 24.2/27.0 1,763 1,618 145 RMS Deviations Average B factor from Ideality Protein Water Bond angles Bond lengths 51.8 Å² 59.0 Å² 1.77° 0.007 Å Ramachandran (φ, ψ) Favored Allowed Generous Disallowed 87.3% 12.2% 0.0% 0.6%

[0163] C. Description of the IgE Structure

[0164] The Cε3 and Cε4 domains of IgE belong to the C1 set of Ig constant domains (Murzin et al., 1995). While the IgE Cε3 and Cε4 domains are individually similar to IgG Cγ2 and Cγ3 domains, respectively, a structure-based sequence alignment of the IgE-Fc and IgG-Fcs reveals several changes in secondary structure (FIG. 7b). Compared to IgE, the IgG contains a single residue insertion (1253 in IgG1) that forms a bulge just after the Cγ2 AB helix. The IgE Cε3 domain lacks a C′ strand and the Cε4 domain has a poorly ordered AB loop in place of the AB helix in Cγ3. Two prolines (P381 and P454) may contribute to the disruption of these secondary structures by altering hydrogen bond capabilities.

[0165] A ribbon diagram of the IgE-Fc is shown in FIG. 8. As in IgG-Fcs, the upper domains (Cε3) of the IgE-Fc do not form any direct protein:protein contacts. The conserved carbohydrate attachment site (N394) faces the cavity between the Cε3 domains. While the observed electron density is consistent with glycosylation at this site, the poor quality of the density precludes modeling of carbohydrate. Inclusion of carbohydrate residues in the model did not decrease the R_(free) or improve the electron density maps. However, the electron density suggests that carbohydrate residues contact each other near the Fc dimer axis, forming the bottom of a narrow cleft between the Cε3 domains. The Cε4 domains form extensive contacts across the dimer interface, burying ˜1,860 Å². Fourteen atomic contacts (<4 Å) formed between the Cε3 and Cε4 domains of a single chain bury 872 Å², and so bury a total of 1,744 Å² in the dimer.

[0166] No electron density for residues N-terminal to V336 (the Cε2-Cε3 linker region) is observed, despite the formation of the interchain disulfide in this region. These Cε2-Cε3 linker residues are ordered in the complex with FcεRI (Garman et al., 2000) and several of these residues interact with the receptor. While the absence of the Cε2 domains may contribute to the disorder of the Cε2-Cε3 linker in the free Fc, the asymmetric binding of linker residues to FcεRI suggests that flexibility is functionally important.

[0167] D. The IgE-Fc Adopts a Novel Conformation

[0168] The crystal structure of the IgE-Fc Cε3-Cε4 domains reveals a novel, closed conformation for antibody effector domains (FIG. 8). In the free IgE-Fc, the Cε3-Cε4 interdomain angle is more acute than that observed between homologous IgG-Fc domains (Deisenhofer et al., 1976; Harris et al., 1999) or in the FcεRI-bound IgE-Fc (open conformation, Garman et al., 2000). Both the relative dispositions of the two Cε3 domains with respect to each other and to the Cε4 domains is altered. In the closed structure, the IgE-Fc Cε3 domains are closer together and slightly rotated with respect to each other. A top view of the Cε3 and Cγ2 domains illustrates differences in the interdomain gap (FIG. 8b). In the IgE-Fc, the distance between the first residue of the Cε3 A strands is only 13 Å. The distance increases to 23 Å in the receptor-bound IgE-Fc, which is similar to the 22 Å observed between the Cγ2 domains in IgG2a-Fc (Harris et al., 1997). The Cε3 domains not only approach each other more closely, but they also lie closer to the Cε4 domains. For example, the top of the Cε3 domain (residue T396 in DE loop) is 23 Å from the top of the Cε4 domain (residue S491). The distance between the corresponding residues in IgG2a is 33 Å, and in the receptor-bound IgE-Fc (open form), the distance is 31 Å. Thus, in the change between the open and closed forms, the top of each Cε3 domain moves 10 Å towards the other Cε3 domain across the dimer axis and 8 Å towards the Cε4 domain of the same chain. The closer approach of the upper domains of IgE (Cε3) to the lower domains (Cε4) decreases the overall height of the IgE-Fc by ˜7 Å compared to the IgG-Fc. The IgE-Fc conformational change is much greater than any differences observed among IgG-Fc crystal structures. Six crystal structures of the IgG-Fc provide nine different observations of a single chain of the IgG-Fc (in three structures, the two chains are constrained by crystallographic symmetry to be identical). These nine IgG-Fc chains, aligned via their Cγ3 domains, reveal IgG-Fc conformational variability as a family of Cγ2 positions (FIG. 9a). In the closed structure, the IgE Cε3 domain lies far outside the range of observed IgG-Fc conformations. When bound to FcεRI, the angle between the Cε3 and Cε4 domains increases and the Cε3 domains approach the observed positions for IgG Cγ2 domains. Some of the structural variation in the IgG-Fcs may be attributable to sequence differences. While the human IgG structures share ˜95% sequence identity and the mouse structures have ˜67% identity, the largest difference in IgG Cγ2 positions occurs between the human and mouse structures which share ˜64% identity (Harris et al., 1999). However, the largest conformational change occurs between the open and closed forms of the IgE-Fc, which are identical in sequence, demonstrating the inherent flexibility of the IgE-Fc.

[0169] E. Analysis of IgE- and IgG-Fc Conformational Flexibility

[0170] The IgE-Fc conformational change can be described by an axis relating the two Ig domains in the open and closed conformations. The program DynDom (Hayward and Berendsen, 1998) defines a rotation of ˜13° and a translation of 1 Å about this axis (arrow in FIG. 9b). Surprisingly, the axis does not lie in the Cε3-Cε4 linker region (436-440) but rather within the Cε3 domain itself, near the Cε3-Cε4 domain interface. Hinge residues that mediate the conformational change lie at both ends of the Cε3 AB helix (residues 343-345 and 351-352) and adjacent to the Cε3-Cε4 linker (residues 435-436). None of the observed IgG-Fc structures exhibit such a large degree of flexibility. Three IgG-Fc structures have been solved in which the two Cγ2 domains of the same Fc exhibit different orientations with respect to their Cγ3 domains (1FC1 (Deisenhofer, 1981), 1IGY (Harris et al., 1998), and 1IGT (Harris et al., 1997)). Since the structural variation occurs within the same Fc, differences due to sequence variation are eliminated. For each structure, DynDom analysis identifies an axis near the Cγ2-Cγ3 interface that describes a motion of 6-7° between the two conformers (FIG. 9c). The orientations of the axes are different from each other and from that of the IgE-Fc, and they describe distinct movements (e.g. side-to-side) of Cγ2. However, none of the IgG motions match the open-to-closed conformational change seen in the IgE-Fc. The different location of the hinge axes and the much smaller range of motion displayed by the IgG-Fc suggest that the flexibility of Ig domains involves multiple factors.

[0171] The change in Cα coordinates between the closed and open conformations of the IgE-Fc is plotted in FIG. 9d. The changes are slightly different for the two Fc chains that bind asymmetrically to the FcεRI (Garman et al., 2000). The Cε3 AB helix (344-352) and the interdomain linker (436-440) remain relatively fixed with respect to the Cε4 domain, while the Cε3 EF helix residues (406-413) show Cα movements of up to 4 Å (FIG. 9a). Positional changes become greater further from the hinge, with the greatest displacement of Cε3 residues observed at the top of the Fc in the BC (363-368), DE (393-395) and FG (422-428) loops that bind to FcεRI (FIG. 9b). Residues in these loops move 7-16 Å between the open and closed conformations (FIG. 9c). Large differences are also observed in the A-strand adjacent to the Cε2-Cε3 linker.

[0172] F. IgE-Fc Carbohydrate

[0173] In both IgE and IgG, a conserved carbohydrate attachment site faces the cavity between the upper domains (Cε3 and Cγ2 respectively). Carbohydrate residues have not been included in the structure, but partial electron density for ˜5 carbohydrate moieties can be observed at the conserved N394 site, branching after the core (-GlcNAc₂Man) into two arms. As in IgG, electron density for carbohydrate lies along the inner face of the protein, shielding hydrophobic residues from solvent (IgE residues Y339, L359, V361). The carbohydrate is not sequestered from solvent, however. In IgE, the carbohydrate attached to N394 can be removed by endoglycosidases under native conditions, suggesting that this region is at least transiently accessible in solution (Basu et al., 1993).

[0174] Carbohydrate is not required for high affinity binding to FcεRI, suggesting that it does not affect the conformation of the IgE-Fc significantly. IgA glycosylation is similarly not required for Fc-receptor binding (Mattu et al., 1998). In contrast, the presence of carbohydrate at a conserved N-linked attachment site in IgG (N297 in IgG1) is critical for maintaining Fc receptor-binding activities (Jefferis et al., 1998). Core glycosylation (-GlcNAc₂Man₃) of IgG, produced in mammalian, yeast and insect cells, is likely sufficient for this carbohydrate function (Jefferis et al., 1998). Functional and biophysical studies of IgG indicate that the carbohydrate moiety has only a limited and local effect on the Fc structure (Jefferis et al., 1998). A comparison of glycosylated and aglycosylated IgG-Fc with a panel of monoclonal antibodies showed no detectable epitope differences, suggesting that global structural changes were not occurring (Walker et al., 1989). ¹H-NMR has been used to study the influence of glycosylation on the structure of IgG-Fc. Histidine resonances were monitored in glycosylated and non-glycosylated IgG-Fc (Lund et al., 1990; Matsuda et al., 1990). Of the five histidines monitored, only one near the conserved glycosylation site (H268 in the Cγ2 BC loop), reported any change in local environment. Histidines at the Cγ2-Cγ3 domain interface did not detect any structural differences. Based on the IgE-Fc:FcεRI crystal structure, the Cγ2 BC loop and DE loop containing the conserved glycosylation site are predicted to participate directly in FcγR interactions (Garman et al., 2000). Local structural changes in these loops could affect receptor binding.

[0175] G. Structural Changes at the Interdomain Interface

[0176] The interdomain interfaces of both IgG-Fc (Cγ2-Cγ3) and IgE-Fc (Cε3-Cε4) are important for Fc function, and structural differences in the interface may influence Fc domain flexibility. Four proteins bind to this region in IgG: neonatal Fc receptor (Burmeister et al., 1994), rheumatoid factor (Corper et al., 1997), Protein A (Deisenhofer, 1981), and Protein G (Sauer-Eriksson et al., 1995). Direct binding of proteins to this region in IgE has not been demonstrated. The binding site for FcεRII has been broadly mapped to the outer surface of Cε3 (Shi et al., 1997; Sutton and Gould, 1993), while the FcεRI binding site is distal to this interface and encompasses the Cε3 BC, DE, and FG loops as well as the Cε2-Cε3 linker (Garman et al., 2000; Henry et al., 1997; Presta et al., 1994). However, despite the fact that residues at the Cε3-Cε4 domain interface do not form direct contacts to the FcεRI, mutations in this region can have a profound effect on FcεRI binding. For example, substitution of IgE Cε3 AB helix residues with IgG Cγ2 AB helix residues disrupts binding, as does a single amino acid mutation, F329A (Presta et al., 1994), suggesting that interactions at the Cε3-Cε4 domain interface are important in maintaining a functional Fc. The AB helix (in Cε3 or Cγ2) mediates the majority of atomic contacts (atoms within 4 Å) between the Fc domains in both IgE and IgG (FIG. 7a). The AB helix contacts adjacent residues and residues in the EF helix of the upper domain. The AB helix also contacts residues in the C, F and G strands and FG loop of the lower Ig domain (Cε4 or Cγ3). Despite the central role of the AB helix in mediating interdomain contacts, AB helix residues are not conserved between IgE and IgG. Only one residue of the helix (εD347, γD262) is invariant (FIG. 7b). In addition, most of the residues that contact the AB helix are not conserved between IgE and IgG. The pattern of contacts made by AB helix residues is different in IgE and IgG. In IgE, most of the contacts made by the AB helix are to residues of the lower (Cε4) domain (15/21 in the open conformation, FIG. 10a). Only one contact is made to the EF helix in the closed form and two additional contacts are formed in the open conformation (dashed lines). In IgG, the majority of the AB helix contacts (12/21) are to other residues within the same Cγ2 domain, with nine contacts to the lower Cγ3 domain. The Cγ2 AB helix forms extensive contacts to the EF helix. Two residues in particular, V263 and H329, form a network of nine contacts within the Cγ2 domain. There are two striking structural features unique to the IgG interdomain interface (FIGS. 9a, 10 d). A single residue insertion after the IgG Cγ2 AB helix, isoleucine 266, forms a distinct bulge at the end of the helix. This isoleucine, together with adjacent residues, forms part of a shallow pocket on the surface of the IgG (FIG. 10d). The second difference in IgG is the presence of a conserved histidine (H329) on the EF helix facing the AB helix. This histidine is completely conserved in IgGs across species and subtypes but is not found in other Ig isotypes. Histidine 329 forms five atomic contacts to the pocket formed by 1266 and neighboring residues (FIG. 10d). The contacts made by H329 are maintained in all IgG-Fc structures, including a highly distorted Fab-Fc hinge-deleted IgG in which the AB helix no longer contacts the lower Ig domain and has shifted away from the Cγ2-Cγ3 domain interface (Guddat et al., 1993). In non-glycosylated IgG-Fc, the ¹H resonances of IgG H329 do not change (Lund et al., 1990; Matsuda et al., 1990), suggesting the preservation of these interactions.

[0177] In contrast, the corresponding residue in IgE, T407, makes two contacts to the AB helix in the open form (FIGS. 10a, 10 c) and makes only one contact and moves away from the AB helix in the closed form (FIGS. 9a, 10 a-c). In rat and mouse IgE sequences T407 is replaced by alanine, suggesting that the conservation of these side chain interactions is not important.

[0178] The extensive contacts formed by the IgG AB helix to other Cγ2 domain residues and the close packing of EF helix residue H329 to the AB helix distinguish the IgG Cγ2-Cγ3 interface. In IgG, the AB helix is more closely associated with the upper (Cγ2) domain than the lower (Cγ3) domain. In contrast, the IgE interface is characterized by extensive interactions of the Cε3 AB helix residues with the lower Cε4 domain residues (FIG. 10a), and contacts with the EF helix are limited. In both IgE Cε3 and IgG Cγ2, the A and B strands separate and do not form hydrogen bonds on either side of the AB helix, allowing for some flexibility in the positioning of the AB helix. However, the flexibility may be limited in IgG by the extensive interactions of the Cγ2 AB and EF helices. In IgE, the limited contacts made between the Cε3 AB and EF helices may allow the helices to move independently.

[0179] H. Effect of the Conformational Change on the FcεRI Binding Site

[0180] The large conformational change of the IgE-Fc structure reorients loops in the Cε3 domains that interact with the high affinity receptor, FcεRI. The large movement of the FcεRI-binding loops suggests that they would be poorly positioned in the closed IgE-Fc structure to interact with the receptor. FIG. 11 shows a molecular surface representation of the open and closed Fc structures, with the receptor-binding residues highlighted in magenta. In the open form, the receptor-binding loops are exposed and the binding residues display a large concave surface that is available to interact with FcεRI. In the closed form, these loops are partially obscured and point towards each other across the IgE-Fc dyad axis, leaving only a narrow gap between the two Cε3 domains that cannot accommodate the binding of the receptor. While the Cε3 BC, DE and FG loops are largely inaccessible in the closed conformation, the disordered Cε2-Cε3 linker residues N-terminal to V336 could form an initial interaction with the receptor even in the closed IgE-Fc structure. Binding of the receptor to linker residues might shift the conformation of the Fc towards the open form, exposing the binding loops.

[0181] I. Structural Basis for the IgE-Fc Conformational Flexibility

[0182] The IgE-Fc structure reveals an unprecedented conformation for antibody effector domains with implications for Fc-receptor binding and therapeutic intervention in human disease. The structure of the closed IgE-Fc suggests that the effector domains of antibody isotypes may have evolved structural characteristics that are associated with isotype-specific biological functions. Structural features that could influence the flexibility of the IgE-Fc include the location and packing of hinge residues and the specific interactions at the Cε3-Cε4 domain interface, such as the position and contacts of the Cε3 AB helix. Other factors that could potentially effect a change in conformation have been considered, such as the specific crystal-packing environment, the presence of high-mannose instead of complex carbohydrate, or the lack of the Cε2 domains. The present invention also includes the solution of a second crystal form of the IgE-Fc containing two IgE-Fc molecules in the asymmetric unit, both in the closed form. These five IgE-Fc chains all adopt a similar conformation, indicating that the closed conformation is not dictated by specific crystal-packing forces.

[0183] It remains to be established whether different carbohydrate structures at the conserved attachment site could influence the extent of the observed IgE-Fc conformational change. Biochemical studies of IgG suggest a limited structural role for the conserved carbohydrate in maintaining the overall three-dimensional arrangement of Fc domains, as discussed above. While functional studies of the IgE-Fc (FcεRIα binding) argue against a significant role for the conserved carbohydrate, structural studies of different IgE-Fc glycoforms may resolve this issue.

[0184] Biochemical and biophysical studies indicate that the IgE-Fc Cε2 domains form a separate structural unit from the Cε3-Cε4 structure solved here. The Cε2-Cε3 linker is susceptible to proteolytic digestion (Perez-Montfort and Metzger, 1982) and adopts an asymmetric conformation upon binding FcεRI (Garman et al., 2000), suggesting that it is accessible and flexible. The presence or absence of the Cε2 domains in the IgE-Fc does not significantly alter the binding constants or thermodynamic parameters (ΔG°, ΔH°, ΔS°, and ΔCp°) of FcεRI binding (Keown et al., 1998). Therefore, the mode of binding to the receptor is likely to be similar for intact IgE-Fc and IgE-Fc Cε3-Cε4. Together, these results suggest that the Cε2 domains have little influence on the structure or conformation of the Cε3 domains.

[0185] Structural characteristics of the IgE Cε3-Cε4 domain interface, as compared to the IgG Cγ2-Cγ3 domain interface, likely enable the conformational flexibility of the IgE-Fc. The AB helix of the first domain (Cε3 or Cγ2) mediates most of the interdomain contacts in the Fc structure and is not conserved in sequence across the five different antibody classes. Packing contacts of the AB helix with the two Fc Ig domains may differ significantly across antibody isotypes, potentially influencing Fc conformation, flexibility and function. The range of conformational flexibility of the Fc domains of different antibody classes could be linked to the evolution of isotype-specific effector functions. The more limited flexibility of IgG structures may reflect similarities in the structural requirements for FcγR and complement (C1q) interactions.

[0186] Other experimental evidence has suggested that IgE adopts a bent configuration in solution and that conformational changes may occur upon binding to FcεRI. The design and interpretation of these experiments could not have anticipated the specific IgE-Fc conformational change of the present invention. Binding of IgE-Fc to FcεRI (Keown et al., 1998) is characterized by a relatively large change in heat capacity (ΔCp°=−815 cal/mol K), which could be in part be caused by IgE-Fc conformational changes. In contrast, binding of IgG-Fc to its homologous low affinity receptor, FcγRIII, exhibits a smaller change in heat capacity (ΔCp°=−360 cal/mol K). Fluorescence energy transfer experiments have shown that the average distance between the N- and C- termini of the IgE is only ˜70 Å, a distance that is possible only if the IgE bends significantly out of the plane of the typical antibody Y- or T-shape (Zheng et al., 1991). Neutron scattering studies have shown that the intact IgE-Fc (Cε2-Cε4) has a significantly more compact shape than a linear arrangement of the domains would allow (Beavil et al., 1995), suggesting that a bend occurs within the IgE-Fc region. The IgE-Fc crystal structure supports the interpretation of bending of the intact IgE at the Cε2-Cε3 linker region, and may provide a better model for the analysis of the neutron scattering data. Experimental tests of IgE flexibility can now be developed based on the structure.

[0187] J. Biological and Therapeutic Implications for IgE-Fc Conformational Flexibility

[0188] Conformational flexibility in the IgE-Fc may be important for unique aspects of IgE biological function. IgE-Fc flexibility may allow induced-fit interactions with FcεRI, contributing to the high affinity binding, and may be important for interactions with the low affinity IgE receptor, FcεRII (FIG. 12). FcεRII is a trimeric C-type lectin that is thought to interact with the IgE-Fc through two of its three lectin domains (Shi et al., 1997). IgG antibodies do not have a corresponding lectin-like receptor, suggesting that the conformational flexibility of the IgE-Fc may be important for this unique antibody-receptor interaction.

[0189] The existence of a closed conformation for the IgE-Fc and the demonstration that the open form binds to the high affinity receptor (Garman et al., 2000) suggest new strategies for the design of inhibitors of the IgE:FcεRI interaction (FIG. 12). Monoclonal antibodies that bind the IgE-Fc and block interactions with FcεRI have demonstrated the therapeutic potential of this approach for the treatment of allergy and asthma (Chang, 2000; Jardieu and Fick, 1999). Stabilization of the closed IgE-Fc conformation by the binding of molecules, either at directly competitive or indirect allosteric sites, could block receptor association, leading to a new class of therapeutic inhibitors for the treatment of IgE-mediated allergic diseases. The IgE Cε3-Cε4 domain interface may provide a target for the binding of small in vitro-selected ligands, as shown for the IgG-Fc (DeLano et al., 2000), that have the potential to act as allosteric inhibitors of receptor binding (FIG. 13). The closed conformation of the IgE-Fc provides the foundation for exploring new routes to alleviating atopic disease and exploring the functional role of Fc domain flexibility in biological effector mechanisms.

[0190] K. Methods

[0191] 1. Expression and Purification of the Human IgE-Fc.

[0192] The expression, purification and characterization of the IgE-Fc from insect cells was performed as described in Example 1.

[0193] 2. Crystallization and Treatment of Crystals

[0194] Purified IgE-Fc was concentrated to 10 mg/ml in 10 mM Tris, pH 8.0, using an ε_(280nm) of 1.32 cm⁻¹ (mg/ml)⁻¹. Crystals were grown in hanging drops using the vapor diffusion method by mixing 0.5 μl protein and 0.5 μl of precipitant (25 mM sodium acetate, pH 4.6, 33% polyethylene glycol [PEG] 4000). Crystals grew at 22° C. in 1-3 days and were sensitive to small changes in salt or PEG concentration and temperature. Crystals were harvested into 25 mM sodium acetate, pH 4.6, 37% PEG 4000, transferred briefly (<30 s) to cryoprotectant solution (harvest solution plus 15% (v/v) ethylene glycol) and cooled rapidly in liquid nitrogen. Crystals belong to the space group P42₁2 (a=b=105.6 Å, c=47.1 Å) and contain one Cε3-Cε4 chain per asymmetric unit. Crystals were transferred serially to higher pH harvest solutions to facilitate metal binding and redox chemistry. Heavy atom screening (˜100 conditions) with a wide range of compounds (27), concentrations (0.1-20 mM) and pH ranges (4.6-8.5) did not yield an isomorphous or anomalous derivative. However, mercury- or platinum-treated crystals diffracted better than native crystals. Based on these observations, crystals were treated with 1 mM copper (II) chloride prior to cooling and data collection. Native crystals diffracted to ˜2.8 Å resolution using a synchrotron source and displayed strong anisotropy and, occasionally, split lattices. Copper-treated crystals diffracted to at least 2.0 Å resolution, with little or no anisotropy. We and others (Basu et al., 1993) have observed that a small fraction of the IgE-Fc does not form the interchain disulfide. The copper II may have oxidized the remaining free cysteines to the disulfide.

[0195] 3. Data Collection, Molecular Replacement and Refinement.

[0196] Data sets were collected at −160° C. from copper-treated crystals at SSRL beamline 7-1 (wtcul) using a Mar300 imaging plate system and at the Advanced Photon Source DND-CAT 5ID beamline (wtcu3) using a MarCCD detector. The data were processed and integrated using the HKL suite of programs (Otwinowski and Minor, 1997). Initial molecular replacement (MR) searches with AMoRe (Collaborative Computational Project, 1994), CNS/XPLOR (Brünger et al., 1998) and EPMR (Kissinger et al., 1999) failed, using a variety of models of IgE based on IgG-Fc structures, including individual Ig domains and a composite model incorporating seven IgG structures. A systematic exploration of the bend, twist and rotation angles of Cε3 relative to Cε4 was then undertaken. A model was constructed from the Cγ2-Cγ3 domains derived from an intact IgG structure (murine IgG2a, PDB entry 1IGT (Harris et al., 1997)), by truncating loops and non-homologous side-chains, resulting in a 144 residue model for the 222 residue IgE-Fc. The Cγ2-Cγ3 linker region of the model was placed at the origin, with Cγ2 and Cγ3 oriented to allow bending to occur about the Z-axis. Rotations around X, Y and Z were applied to the Cγ2 domain (3° steps), while leaving the Cγ3 fixed. Approximately 12,000 models were generated automatically with the program lsqkab (Collaborative Computational Project, 1994) and used in complete AMoRe (Collaborative Computational Project, 1994) searches with the 15-4 Å data from crystal wtcul (Table 7). The models covered an angular range of −30 to +40 degrees around the starting IgG2a structure. A single solution, ˜17° from the starting structure, was found and improved by a local search using 1.0° rotational increments. The finer search yielded a solution with a correlation coefficient of 38% and an R_(factor) of 48.9%. Cycles of model building into simulated-annealing composite-omit electron density maps and refinement were continued with the higher resolution data from crystal wtcu3 using the programs O (Jones et al., 1991) and CNS (Brünger et al., 1998). Refinement was performed against all data from 30-2.3 Å using |F|>0 and an anisotropic bulk solvent correction. Only refinement steps that decreased the R_(free) were accepted. The model includes residues 336-543 and lacks 10 N-terminal and 4 C-terminal residues present in the construct. The receptor binding loops (Cε3 BC, DE, and FG loops) have weaker density and higher B-factors than most of the other residues. Density for the Cε4 AB loop is particularly poor, and this loop was modeled sterically. All of the residues lie within the accepted regions of the Ramachandran plot, with the exception of N481. There is good density for this residue, however, which is in a tight turn that lacks a Gly, Ala, or Ser residue. While some density was for carbohydrate was observed at the N394 site, attempts to build carbohydrate did not improve the R_(free) or the electron density maps, and so it was not included in the model. There is no electron density for the carbohydrate attached to the N371 site. The current refinement statistics are summarized in Table 7. Figures were made using the programs MOLSCRIPT (Kraulis, 1991), GRASP (Nicholls et al., 1991) and Raster 3D (Merritt and Bacon, 1997).

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[0249] While the various embodiments of the present invention have been described in detail, it is apparent that modifications and adaptations of those embodiments will occur to those skilled in the art. It is to be expressly understood, however, that such modifications are adaptations are within the scope of the present invention, as set forth in the following claims.

1 7 1 669 DNA Homo sapiens CDS (1)..(666) 1 gcg gat ccc tgt gat tcc aac ccg aga ggg gtg agc gcc tac cta agc 48 Ala Asp Pro Cys Asp Ser Asn Pro Arg Gly Val Ser Ala Tyr Leu Ser 1 5 10 15 cgg ccc agc ccg ttc gac ctg ttc atc cgc aag tcg ccc acg atc acc 96 Arg Pro Ser Pro Phe Asp Leu Phe Ile Arg Lys Ser Pro Thr Ile Thr 20 25 30 tgt ctg gtg gtg gac ctg gca ccc agc aag ggg acc gtg aac ctg acc 144 Cys Leu Val Val Asp Leu Ala Pro Ser Lys Gly Thr Val Asn Leu Thr 35 40 45 tgg tcc cgg gcc agt ggg aag cct gtg aac cac tcc acc aga aag gag 192 Trp Ser Arg Ala Ser Gly Lys Pro Val Asn His Ser Thr Arg Lys Glu 50 55 60 gag aag cag cgc aat ggc acg tta acc gtc acg tcc acc ctg ccg gtg 240 Glu Lys Gln Arg Asn Gly Thr Leu Thr Val Thr Ser Thr Leu Pro Val 65 70 75 80 ggc acc cga gac tgg atc gag ggg gag acc tac cag tgc agg gtg acc 288 Gly Thr Arg Asp Trp Ile Glu Gly Glu Thr Tyr Gln Cys Arg Val Thr 85 90 95 cac ccc cac ctg ccc agg gcc ctc atg cgg tcc acg acc aag acc agc 336 His Pro His Leu Pro Arg Ala Leu Met Arg Ser Thr Thr Lys Thr Ser 100 105 110 ggc ccg cgt gct gcc ccg gaa gtc tat gcg ttt gcg acg ccg gag tgg 384 Gly Pro Arg Ala Ala Pro Glu Val Tyr Ala Phe Ala Thr Pro Glu Trp 115 120 125 ccg ggg agc cgg gac aag cgc acc ctc gcc tgc ctg atc cag aac ttc 432 Pro Gly Ser Arg Asp Lys Arg Thr Leu Ala Cys Leu Ile Gln Asn Phe 130 135 140 atg cct gag gac atc tcg gtg cag tgg ctg cac aac gag gtg cag ctc 480 Met Pro Glu Asp Ile Ser Val Gln Trp Leu His Asn Glu Val Gln Leu 145 150 155 160 ccg gac gcc cgg cac agc acg acg cag ccc cgc aag acc aag ggc tcc 528 Pro Asp Ala Arg His Ser Thr Thr Gln Pro Arg Lys Thr Lys Gly Ser 165 170 175 ggc ttc ttc gtc ttc agc cgc ctg gag gtg acc agg gcc gaa tgg gag 576 Gly Phe Phe Val Phe Ser Arg Leu Glu Val Thr Arg Ala Glu Trp Glu 180 185 190 cag aaa gat gag ttc atc tgc cgt gca gtc cat gag gca gcg agc ccc 624 Gln Lys Asp Glu Phe Ile Cys Arg Ala Val His Glu Ala Ala Ser Pro 195 200 205 tca cag acc gtc cag cga gcg gtg tct gta aat ccc ggt aaa tga 669 Ser Gln Thr Val Gln Arg Ala Val Ser Val Asn Pro Gly Lys 210 215 220 2 222 PRT Homo sapiens 2 Ala Asp Pro Cys Asp Ser Asn Pro Arg Gly Val Ser Ala Tyr Leu Ser 1 5 10 15 Arg Pro Ser Pro Phe Asp Leu Phe Ile Arg Lys Ser Pro Thr Ile Thr 20 25 30 Cys Leu Val Val Asp Leu Ala Pro Ser Lys Gly Thr Val Asn Leu Thr 35 40 45 Trp Ser Arg Ala Ser Gly Lys Pro Val Asn His Ser Thr Arg Lys Glu 50 55 60 Glu Lys Gln Arg Asn Gly Thr Leu Thr Val Thr Ser Thr Leu Pro Val 65 70 75 80 Gly Thr Arg Asp Trp Ile Glu Gly Glu Thr Tyr Gln Cys Arg Val Thr 85 90 95 His Pro His Leu Pro Arg Ala Leu Met Arg Ser Thr Thr Lys Thr Ser 100 105 110 Gly Pro Arg Ala Ala Pro Glu Val Tyr Ala Phe Ala Thr Pro Glu Trp 115 120 125 Pro Gly Ser Arg Asp Lys Arg Thr Leu Ala Cys Leu Ile Gln Asn Phe 130 135 140 Met Pro Glu Asp Ile Ser Val Gln Trp Leu His Asn Glu Val Gln Leu 145 150 155 160 Pro Asp Ala Arg His Ser Thr Thr Gln Pro Arg Lys Thr Lys Gly Ser 165 170 175 Gly Phe Phe Val Phe Ser Arg Leu Glu Val Thr Arg Ala Glu Trp Glu 180 185 190 Gln Lys Asp Glu Phe Ile Cys Arg Ala Val His Glu Ala Ala Ser Pro 195 200 205 Ser Gln Thr Val Gln Arg Ala Val Ser Val Asn Pro Gly Lys 210 215 220 3 220 PRT Homo sapiens 3 Cys Ala Asp Ser Asn Pro Arg Gly Val Ser Ala Tyr Leu Ser Arg Pro 1 5 10 15 Ser Pro Phe Asp Leu Phe Ile Arg Lys Ser Pro Thr Ile Thr Cys Leu 20 25 30 Val Val Asp Leu Ala Pro Ser Lys Gly Thr Val Asn Leu Thr Trp Ser 35 40 45 Arg Ala Ser Gly Lys Pro Val Asn His Ser Thr Arg Lys Glu Glu Lys 50 55 60 Gln Arg Asn Gly Thr Leu Thr Val Thr Ser Thr Leu Pro Val Gly Thr 65 70 75 80 Arg Asp Trp Ile Glu Gly Glu Thr Tyr Gln Cys Arg Val Thr His Pro 85 90 95 His Leu Pro Arg Ala Leu Met Arg Ser Thr Thr Lys Thr Ser Gly Pro 100 105 110 Arg Ala Ala Pro Glu Val Tyr Ala Phe Ala Thr Pro Glu Trp Pro Gly 115 120 125 Ser Arg Asp Lys Arg Thr Leu Ala Cys Leu Ile Gln Asn Phe Met Pro 130 135 140 Glu Asp Ile Ser Val Gln Trp Leu His Asn Glu Val Gln Leu Pro Asp 145 150 155 160 Ala Arg His Ser Thr Thr Gln Pro Arg Lys Thr Lys Gly Ser Gly Phe 165 170 175 Phe Val Phe Ser Arg Leu Glu Val Thr Arg Ala Glu Trp Glu Gln Lys 180 185 190 Asp Glu Phe Ile Cys Arg Ala Val His Glu Ala Ala Ser Pro Ser Gln 195 200 205 Thr Val Gln Arg Ala Val Ser Val Asn Pro Gly Lys 210 215 220 4 217 PRT Mus musculus 4 Ile Cys Thr Val Pro Glu Val Ser Ser Val Phe Ile Phe Pro Pro Lys 1 5 10 15 Pro Lys Asp Val Leu Thr Ile Thr Leu Thr Pro Lys Val Thr Cys Val 20 25 30 Val Val Asp Ile Ser Lys Asp Asp Pro Glu Val Gln Phe Ser Trp Phe 35 40 45 Val Asp Asp Val Glu Val His Thr Ala Gln Thr Gln Pro Arg Glu Glu 50 55 60 Gln Phe Asn Ser Thr Phe Arg Ser Val Ser Glu Leu Pro Ile Met His 65 70 75 80 Gln Asp Trp Leu Asn Gly Lys Glu Phe Lys Cys Arg Val Asn Ser Ala 85 90 95 Ala Phe Pro Ala Pro Ile Glu Lys Thr Ile Ser Lys Thr Lys Gly Arg 100 105 110 Pro Lys Ala Pro Gln Val Tyr Thr Ile Pro Pro Pro Lys Glu Gln Met 115 120 125 Ala Lys Asp Lys Val Ser Leu Thr Cys Met Ile Thr Asp Phe Phe Pro 130 135 140 Glu Asp Ile Thr Val Glu Trp Gln Trp Asn Gly Gln Pro Ala Glu Asn 145 150 155 160 Tyr Lys Asn Thr Gln Pro Ile Met Asn Thr Asn Gly Ser Tyr Phe Val 165 170 175 Tyr Ser Lys Leu Asn Val Gln Lys Ser Asn Trp Glu Ala Gly Asn Thr 180 185 190 Phe Thr Cys Ser Val Leu His Glu Gly Leu His Asn His His Thr Glu 195 200 205 Lys Ser Leu Ser His Ser Pro Gly Lys 210 215 5 219 PRT Mus musculus 5 Cys Pro Ala Pro Asn Leu Leu Gly Gly Pro Ser Val Phe Ile Phe Pro 1 5 10 15 Pro Lys Ile Lys Asp Val Leu Met Ile Ser Leu Ser Pro Ile Val Thr 20 25 30 Cys Val Val Val Asp Val Ser Glu Asp Asp Pro Asp Val Gln Ile Ser 35 40 45 Trp Phe Val Asn Asn Val Glu Val His Thr Ala Gln Thr Gln Thr His 50 55 60 Arg Glu Asp Tyr Asn Ser Thr Leu Arg Val Val Ser Ala Leu Pro Ile 65 70 75 80 Gln His Gln Asp Trp Met Ser Gly Lys Glu Phe Lys Cys Lys Val Asn 85 90 95 Asn Lys Asp Leu Pro Ala Pro Ile Glu Arg Thr Ile Ser Lys Pro Lys 100 105 110 Gly Ser Val Arg Ala Pro Gln Val Tyr Val Leu Pro Pro Pro Glu Glu 115 120 125 Glu Met Thr Lys Lys Gln Val Thr Leu Thr Cys Met Val Thr Asp Phe 130 135 140 Met Pro Glu Asp Ile Tyr Val Glu Trp Thr Asn Asn Gly Lys Thr Glu 145 150 155 160 Leu Asn Tyr Lys Asn Thr Glu Pro Val Leu Asp Ser Asp Gly Ser Tyr 165 170 175 Phe Met Tyr Ser Lys Leu Arg Val Glu Lys Lys Asn Trp Val Glu Arg 180 185 190 Asn Ser Tyr Ser Cys Ser Val Val His Glu Gly Leu His Asn His His 195 200 205 Thr Thr Lys Ser Phe Ser Arg Thr Pro Gly Lys 210 215 6 219 PRT Homo sapiens 6 Cys Pro Ala Pro Glu Phe Leu Gly Gly Pro Ser Val Phe Leu Phe Pro 1 5 10 15 Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr Pro Glu Val Thr 20 25 30 Cys Val Val Val Asp Val Ser Gln Glu Asp Pro Glu Val Gln Phe Asn 35 40 45 Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys Thr Lys Pro Arg 50 55 60 Glu Glu Gln Phe Asn Ser Thr Tyr Arg Val Val Ser Val Leu Thr Val 65 70 75 80 Leu His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys Cys Lys Val Ser 85 90 95 Asn Lys Gly Leu Pro Ser Ser Ile Glu Lys Thr Ile Ser Lys Ala Lys 100 105 110 Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro Pro Ser Gln Glu 115 120 125 Glu Met Thr Lys Asn Gln Val Ser Leu Thr Cys Leu Val Lys Gly Phe 130 135 140 Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn Gly Gln Pro Glu 145 150 155 160 Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser Asp Gly Ser Phe 165 170 175 Phe Leu Tyr Ser Arg Leu Thr Val Asp Lys Ser Arg Trp Gln Glu Gly 180 185 190 Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu His Asn His Tyr 195 200 205 Thr Gln Lys Ser Leu Ser Leu Ser Leu Gly Lys 210 215 7 219 PRT Homo sapiens 7 Cys Pro Ala Pro Glu Leu Leu Gly Gly Pro Ser Val Phe Leu Phe Pro 1 5 10 15 Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr Pro Glu Val Thr 20 25 30 Cys Val Val Val Asp Val Ser His Glu Asp Pro Glu Val Lys Phe Asn 35 40 45 Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys Thr Lys Pro Arg 50 55 60 Glu Glu Gln Tyr Asn Ser Thr Tyr Arg Val Val Ser Val Leu Thr Val 65 70 75 80 Leu His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys Cys Lys Val Ser 85 90 95 Asn Lys Ala Leu Pro Ala Pro Ile Glu Lys Thr Ile Ser Lys Ala Lys 100 105 110 Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro Pro Ser Arg Asp 115 120 125 Glu Leu Thr Lys Asn Gln Val Ser Leu Thr Cys Leu Val Lys Gly Phe 130 135 140 Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn Gly Gln Pro Glu 145 150 155 160 Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser Asp Gly Ser Phe 165 170 175 Phe Leu Tyr Ser Lys Leu Thr Val Asp Lys Ser Arg Trp Gln Gln Gly 180 185 190 Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu His Asn His Tyr 195 200 205 Thr Gln Lys Ser Leu Ser Leu Ser Pro Gly Lys 210 215 

What is claimed is:
 1. A three-dimensional model selected from the group consisting of: (a) a three-dimensional model of a human IgE Fc region comprising Cε3 and Cε4 domains (Fc-Cε3/Cε4), wherein said model substantially represents the atomic coordinates specified in a Table selected from the group consisting of Table 1, Table 2 and Table 3; and (b) a three-dimensional model comprising a modification of said model of (a), wherein said modification represents an antibody Fc region that binds to a FcεRIα protein.
 2. A method to produce the three-dimensional model of claim 1, wherein the three-dimensional model represents the Fc-Cε3/Cε4 region of a human IgE antibody, said method comprising representing amino acids of said region at substantially the atomic coordinates specified in a Table selected from the group consisting of Table 1, Table 2 and Table
 3. 3. A method to produce a three-dimensional model of a FcεRIα binding domain other than a human FcεRIα binding domain represented by the three-dimensional model substantially representing the atomic coordinates specified in claim 1, said method comprising homology modeling.
 4. An isolated crystal of a Fc-Cε3/Cε4 region of a human IgE antibody.
 5. A method to produce the isolated crystal of claim 4, said method comprising vapor diffusion.
 6. An isolated Fc-Cε3/Cε4 protein selected from the group consisting of: (a) a protein consisting of SEQ ID NO:2; and (b) a homologous protein that is structurally homologous to a protein of (a), wherein said homologous protein binds to a FcεRIα protein.
 7. A nucleic acid molecule comprising a nucleic acid sequence that encodes said isolated Fc-Cε3/Cε4 protein of claim
 6. 8. A recombinant molecule comprising the nucleic acid sequence of claim
 7. 9. A recombinant virus comprising the nucleic acid sequence of claim
 7. 10. A recombinant cell comprising the nucleic acid sequence of claim
 7. 11. A method to produce a protein comprising culturing the recombinant cell of claim
 10. 12. A method to identify a compound that inhibits the binding between an IgE antibody and a FcεRIα protein, said method comprising using a three-dimensional model of a Fc-Cε3/Cε4 region of a human IgE to identify said compound, wherein said model substantially represents the atomic coordinates specified in a Table selected from the group consisting of Table 1, Table 2 and Table
 3. 13. An inhibitory compound identified in accordance with the method of claim
 12. 14. A therapeutic composition comprising the inhibitory compound of claim
 13. 15. A method to protect an animal from allergy, said method comprising administering to said animal the inhibitory compound of claim
 13. 16. A method to improve a function of an antibody comprising a Fc-Cε3/Cε4 region, said improved function being selected from the group consisting of increased stability, increased affinity for an IgE binding domain of a FcεRIα protein, altered substrate specificity, and increased solubility, said method comprising: (a) analyzing a three-dimensional model substantially representing the atomic coordinates specified in a Table selected from the group consisting of Table 1, Table 2 and Table 3 to identify at least one amino acid of the Fc-Cε3/Cε4 region represented by said model which if replaced by said identified amino acid(s) improves at least one of said functions of said Fc-Cε3/Cε4 region; and (b) replacing said identified amino acid(s) to produce a mutein having at least one of said improved functions.
 17. A mutein produced by the method of claim 16, wherein said mutein has an improved function compared to a Fc-Cε3/Cε4 protein comprising amino acid sequence SEQ ID NO:2, wherein said improved function is selected from the group consisting increased stability compared to the stability of a human IgE Fc region comprising amino acid sequence SEQ ID NO:2, increased affinity for a FcεRIα protein compared to the FcεRIα affinity of a human IgE Fc region comprising amino acid sequence SEQ ID NO:2, altered substrate affinity compared to the affinity for human FcεRIα of a human IgE Fc region comprising amino acid sequence SEQ ID NO:2, and increased solubility compared to the solubility of a human IgE Fc region comprising amino acid sequence SEQ ID NO:2.
 18. A polypeptide selected from the group consisting of a FcεRIα binding domain, an interdomain groove between the two Cε3/Cε4 domains of said antibody Fc region, a hinge between Cε3 and Cε4 domains of said antibody Fc region, and a region of a Cε3 or Cε4 domain, the relative position of which changes by greater than 1 angstrom between closed and receptor-bound Fc-Cε3/Cε4 conformations.
 19. The polypeptide of claim 18, wherein said composition is selected from the group consisting of a linker between Cε2 and Cε3, a BC loop of Cε3, a DE loop of Cε3, and a FG loop of Cε3, a loop or strand defining the interdomain groove, a AB helix of Cε3 and, a region lying above said AB helix of Cε3.
 20. An isolated nucleic acid molecule encoding the polypeptide of claim
 18. 